Food and Drug Administration#Organizational structure

{{Tree list}}

• Department of Health and Human Services
• {{Tree list/final branch}}Food and Drug Administration
• Office of the Commissioner (C)
• Office of the Chief Counsel (OCC)
• Office of the Executive Secretariat (OES)
• Office of the Counselor to the Commissioner
• {{Tree list/final branch}} Office of Digital Transformation (ODT)
• Center for Biologics Evaluation and Research (CBER)
• Center for Devices and Radiological Health (CDRH)
• Center for Drug Evaluation and Research (CDER)
• Center for Food Safety and Applied Nutrition (CFSAN)
• Center for Tobacco Products (CTP)
• Center for Veterinary Medicine (CVM)
• Oncology Center of Excellence (OCE)
• Office of Regulatory Affairs (ORA)
• Office of Clinical Policy and Programs (OCPP)
• Office of External Affairs (OEA)
• Office of Food Policy and Response (OFPR)
• Office of Minority Health and Health Equity (OMHHE)
• Office of Operations (OO)
• Office of Policy, Legislation, and International Affairs (OPLIA)
• Office of the Chief Scientist (OCS)
• {{Tree list/final branch}}National Center for Toxicological Research (NCTR)
• Office of Women's Health (OWH)

{{Tree list/end}}

File:FDA Building 66 - CDRH (5160772175).jpg.|alt=]]

FDA headquarters facilities are currently located in Montgomery County and Prince George's County, Maryland.{{Cite web |date=April 27, 2020 |title=Buildings and Facilities |url=https://www.fda.gov/about-fda/jobs-and-training-fda/buildings-and-facilities |access-date=October 3, 2020 |website=U.S. Food and Drug Administration |language=en |archive-date=April 21, 2020 |archive-url=https://web.archive.org/web/20200421020851/https://www.fda.gov/about-fda/jobs-and-training-fda/buildings-and-facilities |url-status=dead}}

Since 1990, the FDA has had employees and facilities on {{Convert|130|acre|ha|abbr=off}} of the White Oak Federal Research Center in the White Oak area of Silver Spring, Maryland.Coordinates of FDA Headquarters at White Oak, Maryland: {{coord|39.0353363|-76.9830894|region:US-MD_type:landmark|format=dms|name=FDA Headquarters at White Oak, Maryland}} In 2001, the General Services Administration (GSA) began new construction on the campus to consolidate the FDA's 25 existing operations in the Washington metropolitan area, its headquarters in Rockville, and several fragmented office buildings. The first building, the Life Sciences Laboratory, was dedicated and opened with 104 employees in December 2003. {{as of|December 2018|post=,}} the FDA campus has a population of 10,987 employees housed in approximately {{Convert|3800000|sqft|m2|abbr=off}} of space, divided into ten offices and four laboratory buildings. The campus houses the Office of the Commissioner (OC), the Office of Regulatory Affairs (ORA),  the Center for Drug Evaluation and Research (CDER), the Center for Devices and Radiological Health (CDRH), the Center for Biologics Evaluation and Research (CBER) and offices for the Center for Veterinary Medicine (CVM).

With the passing of the FDA Reauthorization Act of 2017, the FDA projects a 64% increase in employees to 18,000 over the next 15 years and wants to add approximately {{Convert|1600000|sqft|m2|abbr=off}} of office and special use space to their existing facilities. The National Capital Planning Commission approved a new master plan for this expansion in December 2018,{{Cite web |title=FDA White Oak Master Plan |url=https://www.ncpc.gov/projects/MP201/ |access-date=October 3, 2020 |website=National Capital Planning Commission |language=en |archive-date=October 9, 2020 |archive-url=https://web.archive.org/web/20201009032259/https://www.ncpc.gov/projects/MP201/ |url-status=live}} and construction is expected to be completed by 2035, dependent on GSA appropriations.{{cite journal |url=https://www.fda.gov/AboutFDA/WorkingatFDA/BuildingsandFacilities/WhiteOakCampusInformation/ucm057328.htm |title=White Oak Campus Project Schedule |journal=FDA |date=October 8, 2015 |access-date=December 16, 2019 |archive-date=April 23, 2019 |archive-url=https://web.archive.org/web/20190423052101/https://www.fda.gov/AboutFDA/WorkingatFDA/BuildingsandFacilities/WhiteOakCampusInformation/ucm057328.htm |url-status=dead}}

File:Toxicology Research at FDA (NCTR Campus) (6023336064).jpg is the headquarters of the National Center for Toxicological Research.]]

The Office of Regulatory Affairs is considered the agency's "eyes and ears", conducting the vast majority of the FDA's work in the field.{{Cite web |title=Key FDA Policies for Medical Device Manufacturer Inspections |url=https://www.nsf.org/knowledge-library/key-fda-policies-procedures-practices-before-during-after-medical-device-manufacturer-inspections |access-date=January 2, 2025 |website=www.nsf.org |language=en}} Its employees, known as Consumer Safety Officers, or more commonly known simply as investigators, inspect production, warehousing facilities, investigate complaints, illnesses, or outbreaks, and review documentation in the case of medical devices, drugs, biological products, and other items where it may be difficult to conduct a physical examination or take a physical sample of the product. The Office of Regulatory Affairs is divided into five regions, which are further divided into 20 districts. The districts are based roughly on the geographic divisions of the Federal court system. Each district comprises a main district office and a number of Resident Posts, which are FDA remote offices that serve a particular geographic area. ORA also includes the Agency's network of regulatory laboratories, which analyze any physical samples taken. Though samples are usually food-related, some laboratories are equipped to analyze drugs, cosmetics, and radiation-emitting devices.

File:US Food and Drug Administration Office 20180930.jpg

The Office of Criminal Investigations was established in 1991 to investigate criminal cases. To do so, OCI employs approximately 200 Special Agents nationwide who, unlike ORA Investigators, are armed, have badges, and do not focus on technical aspects of the regulated industries. Rather, OCI agents pursue and develop cases when individuals and companies commit criminal actions, such as fraudulent claims or knowingly and willfully shipping known adulterated goods in interstate commerce. In many cases, OCI pursues cases involving violations of Title 18 of the United States Code (e.g., conspiracy, false statements, wire fraud, mail fraud), in addition to prohibited acts as defined in Chapter III of the FD&C Act. OCI Special Agents often come from other criminal investigations backgrounds, and frequently work closely with the Federal Bureau of Investigation, Assistant Attorney General, and even Interpol. OCI receives cases from a variety of sources—including ORA, local agencies, and the FBI, and works with ORA Investigators to help develop the technical and science-based aspects of a case.{{Cite journal | author = Office of Regulatory Affairs |date=October 7, 2021 |title=About OCI |url=https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/criminal-investigations/about-oci |journal=FDA |language=en |access-date=January 14, 2023 |archive-date=January 14, 2023 |archive-url=https://web.archive.org/web/20230114025654/https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/criminal-investigations/about-oci |url-status=dead }}

The FDA has a number of field offices across the United States, in addition to international locations in China, India, Europe, the Middle East, and Latin America.{{cite web |author= |date=May 21, 2020 |title=Buildings and Facilities |url=https://www.fda.gov/about-fda/jobs-and-training-fda/buildings-and-facilities |url-status=live |archive-url=https://web.archive.org/web/20200421020851/https://www.fda.gov/about-fda/jobs-and-training-fda/buildings-and-facilities |archive-date=April 21, 2020 |access-date=May 20, 2020 | publisher = U.S. Food and Drug Administration |language=en}}

As of 2021, the FDA had responsibility for overseeing $2.7 trillion in food, medical, and tobacco products. Some 54% of its budget derives from the federal government, and 46% is covered by industry user fees for FDA services.{{Cite web |publisher=US Food and Drug Administration |date=November 26, 2021 |title=Fact Sheet: FDA at a Glance |url=https://www.fda.gov/economics-staff/fda-glance |access-date=February 21, 2022 |archive-date=February 24, 2022 |archive-url=https://web.archive.org/web/20220224041029/https://www.fda.gov/about-fda/fda-basics/fact-sheet-fda-glance |url-status=live }} For example, pharmaceutical firms pay fees to expedite drug reviews.

According to Forbes, pharmaceutical firms provide 75% of the FDA's drug review budget.{{Cite news |date=September 15, 2022 |title=F.D.A.'s Drug Industry Fees Fuel Concerns Over Influence |url=https://www.nytimes.com/2022/09/15/health/fda-drug-industry-fees.html |work=NY Times}}{{Cite web | vauthors = LaMattina J |date=June 28, 2018 |title=The Biopharmaceutical Industry Provides 75% Of The FDA's Drug Review Budget. Is This A Problem? |url=https://www.forbes.com/sites/johnlamattina/2018/06/28/the-biopharmaceutical-industry-provides-75-of-the-fdas-drug-review-budget-is-this-a-problem/ |url-status=live |archive-url=https://archive.today/20230103040036/https://www.forbes.com/sites/johnlamattina/2018/06/28/the-biopharmaceutical-industry-provides-75-of-the-fdas-drug-review-budget-is-this-a-problem/?sh=717a057449ec |archive-date=January 3, 2023 |access-date=January 3, 2023 |website=Forbes |language=en}}

Emergency Use Authorization (EUA) is a mechanism that was created to facilitate the availability and use of medical countermeasures, including vaccines and personal protective equipment, during public health emergencies such as the Zika virus epidemic, the Ebola virus epidemic and the COVID-19 pandemic.{{Cite journal | author = Office of the Commissioner |date=August 31, 2021 |title=Emergency Use Authorization--Archived Information |url=https://www.fda.gov/emergency-preparedness-and-response/mcm-legal-regulatory-and-policy-framework/emergency-use-authorization-archived-information |journal=FDA |language=en |access-date=September 10, 2021 |archive-date=June 15, 2020 |archive-url=https://web.archive.org/web/20200615170705/https://www.fda.gov/emergency-preparedness-and-response/mcm-legal-regulatory-and-policy-framework/emergency-use-authorization-archived-information |url-status=dead }}

The programs for safety regulation vary widely by the type of product, its potential risks, and the regulatory powers granted to the agency. For example, the FDA regulates almost every facet of prescription drugs, including testing, manufacturing, labeling, advertising, marketing, efficacy, and safety—yet FDA regulation of cosmetics focuses primarily on labeling and safety. The FDA regulates most products with a set of published standards enforced by a modest number of facility inspections. Inspection observations are documented on Form 483.{{Cite journal |date=November 21, 2022 |title=Inspection Observations |url=https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/inspection-references/inspection-observations |journal=Fda.gov |language=en |access-date=January 14, 2023 |archive-date=January 14, 2023 |archive-url=https://web.archive.org/web/20230114025900/https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/inspection-references/inspection-observations |url-status=dead }}

In June 2018, the FDA released a statement regarding new guidelines to help food and drug manufacturers "implement protections against potential attacks on the U.S. food supply".{{cite press release |url=https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm611177.htm |title=Statement from FDA Commissioner Scott Gottlieb, M.D., on new guidance to help manufacturers implement protections against potential attacks on the U.S. food supply |publisher=Food and Drug Administration | vauthors = Gottlieb S |date=June 19, 2018 |access-date=June 20, 2018 |archive-date=July 24, 2018 |archive-url=https://web.archive.org/web/20180724202237/https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm611177.htm |url-status=dead}} One of the guidelines includes the Intentional Adulteration (IA) rule, which requires strategies and procedures by the food industry to reduce the risk of compromise in facilities and processes that are significantly vulnerable.{{Cite web |title=Federal Register :: Request Access |url=https://unblock.federalregister.gov/ |access-date=January 14, 2023 |website=unblock.federalregister.gov |archive-date=June 5, 2023 |archive-url=https://web.archive.org/web/20230605020052/https://unblock.federalregister.gov/ |url-status=live }}{{Cite journal | author = Center for Food Safety and Applied Nutrition |date=September 9, 2020 |title=Full Text of the Food Safety Modernization Act (FSMA) |url=https://www.fda.gov/food/food-safety-modernization-act-fsma/full-text-food-safety-modernization-act-fsma |journal=FDA |language=en |access-date=January 14, 2023 |archive-date=September 12, 2018 |archive-url=https://web.archive.org/web/20180912032805/https://www.fda.gov/Food/GuidanceRegulation/FSMA/ucm247548.htm |url-status=dead }}

The FDA also uses tactics of regulatory shaming,{{Cite journal | vauthors = Yadin S |date=2019 |title=Regulatory Shaming |journal=Environmental Law (Lewis & Clark) |volume=49 |page=41 |ssrn=3290017}} mainly through online publication of non-compliance, warning letters, and "shaming lists." Regulation by shaming harnesses firms' sensitivity to reputational damage. For example, in 2018, the agency published an online "black list", in which it named dozens of branded drug companies that are supposedly using unlawful or unethical means to attempt to impede competition from generic drug companies.{{Cite journal | vauthors = Yadin S |date=2019 |title=Shaming Big Pharma |url=http://yalejreg.com/shaming-big-pharma/ |journal=Yale Journal on Regulation Bulletin |volume=36 |page=17 |access-date=May 18, 2019 |archive-date=May 18, 2019 |archive-url=https://web.archive.org/web/20190518100524/http://yalejreg.com/shaming-big-pharma/ |url-status=live}}

The FDA frequently works with other federal agencies, including the Department of Agriculture, the Drug Enforcement Administration, Customs and Border Protection, and the Consumer Product Safety Commission. They also often work with local and state government agencies in performing regulatory inspections and enforcement actions.{{Cite journal |date=October 7, 2022 |title=What does FDA regulate? |url=https://www.fda.gov/about-fda/fda-basics/what-does-fda-regulate |journal=FDA |language=en |access-date=January 14, 2023 |archive-date=January 14, 2023 |archive-url=https://web.archive.org/web/20230114030432/https://www.fda.gov/about-fda/fda-basics/what-does-fda-regulate |url-status=dead }}

{{Main|Regulation of food and dietary supplements by the U.S. Food and Drug Administration}}

The regulation of food and dietary supplements by the Food and Drug Administration is governed by various statutes enacted by the United States Congress and interpreted by the FDA. Pursuant to the Federal Food, Drug, and Cosmetic Act and accompanying legislation, the FDA has authority to oversee the quality of substances sold as food in the United States, and to monitor claims made in the labeling of both the composition and the health benefits of foods.

The FDA subdivides substances that it regulates as food into various categories—including foods, food additives, added substances (human-made substances that are not intentionally introduced into food, but nevertheless end up in it), and dietary supplements. Dietary supplements or dietary ingredients include vitamins, minerals, herbs, amino acids, and enzymes.{{Cite web |url=http://www.fda.gov/food/dietary-supplements/dietary-supplement-products-ingredients |title=Dietary Supplement Products & Ingredients | author = Center for Food Safety and Applied Nutrition |date=March 17, 2020 | publisher = U.S. Food and Drug Administration |language=en |access-date=April 2, 2020 |archive-date=May 28, 2020 |archive-url=https://web.archive.org/web/20200528034323/https://www.fda.gov/food/dietary-supplements/dietary-supplement-products-ingredients |url-status=dead}} Specific standards the FDA exercises differ from one category to the next. Furthermore, legislation had granted the FDA a variety of means to address violations of standards for a given substance category.

Under the Dietary Supplement Health and Education Act of 1994 (DSHEA), the FDA is responsible for ensuring that manufacturers and distributors of dietary supplements and dietary ingredients meet the current requirements. These manufacturers and distributors are not allowed to advertise their products in an adulterated way, and they are responsible for evaluating the safety and labeling of their product.{{Cite web |url=http://www.fda.gov/food/dietary-supplements |title=Dietary Supplements | work = Center for Food Safety and Applied Nutrition |date=February 4, 2020 | publisher = U.S Food and Drug Administration |language=en |access-date=April 2, 2020 |archive-date=April 3, 2020 |archive-url=https://web.archive.org/web/20200403035844/https://www.fda.gov/food/dietary-supplements |url-status=dead}}

The FDA has a "Dietary Supplement Ingredient Advisory List" that includes ingredients that sometimes appear on dietary supplements but need further evaluation.{{cite web |title=Dietary Supplement Ingredient Advisory List |publisher=U.S. Food & Drug Administration |url=https://www.fda.gov/food/dietary-supplement-products-ingredients/dietary-supplement-ingredient-advisory-list |access-date=May 10, 2020 |archive-date=September 25, 2020 |archive-url=https://web.archive.org/web/20200925213510/https://www.fda.gov/food/dietary-supplement-products-ingredients/dietary-supplement-ingredient-advisory-list |url-status=dead}} An ingredient is added to this list when it is excluded from use in a dietary supplement, does not appear to be an approved food additive or recognized as safe, and/or is subjected to the requirement for pre-market notification without having a satisfied requirement.{{Cite web | work = Center for Food Safety and Applied Nutrition |date=December 20, 2019 |title=Dietary Supplement Ingredient Advisory List |url=http://www.fda.gov/food/dietary-supplement-products-ingredients/dietary-supplement-ingredient-advisory-list | publisher = U.S. Food and Drug Administration |language=en |access-date=April 2, 2020 |archive-date=April 16, 2020 |archive-url=https://web.archive.org/web/20200416023320/https://www.fda.gov/food/dietary-supplement-products-ingredients/dietary-supplement-ingredient-advisory-list |url-status=dead}}

The FDA does not approve applied coatings used in the food processing industry.{{cite web | url = http://www.decc.com/fda-acceptable-vs-fda-approved.php | title = FDA Approved Coatings vs. FDA Acceptable Coatings | work = DECC Company | archive-url = https://web.archive.org/web/20130911093254/http://www.decc.com/fda-acceptable-vs-fda-approved.php | archive-date=September 11, 2013 | access-date = October 23, 2013 }} There is no review process to approve the composition of nonstick coatings; nor does the FDA inspect or test these materials. Through their governing of processes, however, the FDA does have a set of regulations that cover the formulation, manufacturing, and use of nonstick coatings. Hence, materials like Polytetrafluoroethylene (Teflon) are not and cannot be considered as FDA Approved, but rather, they are a "FDA Compliant" or "FDA Acceptable".

{{Further|Biosecurity|Bioterrorism|Biosecurity in the United States}}

Medical countermeasures (MCMs) are products such as biologics and pharmaceutical drugs that can protect from or treat the health effects of a chemical, biological, radiological, or nuclear (CBRN) attack. MCMs can also be used for prevention and diagnosis of symptoms associated with CBRN attacks or threats.{{cite web |title=What are Medical Countermeasures? |url=https://www.fda.gov/EmergencyPreparedness/Counterterrorism/MedicalCountermeasures/AboutMCMi/ucm431268.htm | publisher = U.S. Food and Drug Administ ration: Emergency Preparedness and Response |access-date=June 15, 2016 |archive-date=April 22, 2019 |archive-url=https://web.archive.org/web/20190422171542/https://www.fda.gov/EmergencyPreparedness/Counterterrorism/MedicalCountermeasures/AboutMCMi/ucm431268.htm |url-status=dead}} The FDA runs a program called the "FDA Medical Countermeasures Initiative" (MCMi), with programs funded by the federal government. It helps support "partner" agencies and organisations prepare for public health emergencies that could require MCMs.{{cite news |title=Alliance for Biosecurity applauds subcommittee efforts to sustain medical countermeasure funding |url=https://homelandprepnews.com/biological-threats/bioterrorism/18984-alliance-biosecurity-applauds-subcommittee-efforts-sustain-medical-countermeasure-funding/ |access-date=June 15, 2016 |work=Homeland Preparedness News |date=June 8, 2016 |location=Washington, D.C. |archive-date=January 28, 2021 |archive-url=https://web.archive.org/web/20210128183519/https://homelandprepnews.com/stories/18984-alliance-biosecurity-applauds-subcommittee-efforts-sustain-medical-countermeasure-funding/ |url-status=live}}

File:FDA Bldg 51 - Main Entrance (5161374834).jpg.|alt=]]

The Center for Drug Evaluation and Research uses different requirements for the three main drug product types: new drugs, generic drugs, and over-the-counter drugs. A drug is considered "new" if it is made by a different manufacturer, uses different excipients or inactive ingredients, is used for a different purpose, or undergoes any substantial change. The most rigorous requirements apply to new molecular entities: drugs that are not based on existing medications.{{Cite web |date=June 21, 2022 |title=Center for Drug Evaluation and Research {{!}} CDER |url=https://www.fda.gov/about-fda/fda-organization/center-drug-evaluation-and-research-cder |access-date=January 14, 2023 | publisher = U.S. Food and Drug Administ ration |language=en |archive-date=January 14, 2023 |archive-url=https://web.archive.org/web/20230114030540/https://www.fda.gov/about-fda/fda-organization/center-drug-evaluation-and-research-cder |url-status=live }}

{{more citations needed section|date=August 2019}}

New drugs receive extensive scrutiny before FDA approval in a process called a new drug application (NDA).{{cite web |url=https://www.fda.gov/Drugs/DevelopmentApprovalProcess/HowDrugsareDevelopedandApproved/ApprovalApplications/NewDrugApplicationNDA/ |title=New Drug Application (NDA) |publisher=Food and Drug Administration |access-date=November 20, 2012 |archive-date=November 1, 2013 |archive-url=https://web.archive.org/web/20131101115332/http://www.fda.gov/Drugs/DevelopmentApprovalProcess/HowDrugsareDevelopedandApproved/ApprovalApplications/NewDrugApplicationNDA/ |url-status=dead}} Under the Presidency of Donald Trump, the agency has worked to make the drug-approval process go faster.{{Cite journal | vauthors = Van Loo R |date=August 1, 2018 |title=Regulatory Monitors: Policing Firms in the Compliance Era |url=https://scholarship.law.bu.edu/faculty_scholarship/265 |journal=Faculty Scholarship |volume=119 |issue=2 |page=369 |access-date=October 10, 2020 |archive-date=June 4, 2020 |archive-url=https://web.archive.org/web/20200604022358/https://scholarship.law.bu.edu/faculty_scholarship/265/ |url-status=live}}{{rp|10}} Critics, however, argue that FDA standards are not sufficiently rigorous to prevent unsafe or ineffective drugs from getting approval.{{citation |title=Medical Nihilism | vauthors = Stegenga J |publisher=Oxford University Press |year=2018 |isbn=978-0-19-874704-8 |url=https://global.oup.com/academic/product/medical-nihilism-9780198747048?cc=hr&lang=en& |access-date=April 20, 2018 |archive-date=December 11, 2019 |archive-url=https://web.archive.org/web/20191211120725/https://global.oup.com/academic/product/medical-nihilism-9780198747048?cc=hr&lang=en& |url-status=live}} New drugs are available only by prescription by default. A change to over-the-counter (OTC) status is a separate process, and the drug must be approved through an NDA first. A drug that is approved is said to be "safe and effective when used as directed". Drugs being produced by a new manufacturer can be approved through one of two faster processes: the Abbreviated New Drug Application (ANDA) or the 505(b)(2) regulatory pathway for complex generic or biosimilar medications.{{Cite journal|author=Center for Drug Evaluation and Research|date=August 9, 2024 |title=Abbreviated Approval Pathways for Drug Product: 505(b)(2) or ANDA? |url=https://www.fda.gov/drugs/cder-small-business-industry-assistance-sbia/abbreviated-approval-pathways-drug-product-505b2-or-anda |archive-url=https://web.archive.org/web/20220519201501/https://www.fda.gov/drugs/cder-small-business-industry-assistance-sbia/abbreviated-approval-pathways-drug-product-505b2-or-anda |url-status=dead |archive-date=May 19, 2022 |journal=FDA |language=en}}

Very rare, limited exceptions to this multi-step process involving animal testing and controlled clinical trials can be granted out of compassionate use protocols. This was the case during the 2015 Ebola epidemic with the use, by prescription and authorization, of ZMapp and other experimental treatments, and for new drugs that can be used to treat debilitating and/or very rare conditions for which no existing remedies or drugs are satisfactory, or where there has not been an advance in a long period of time. The studies are progressively longer, gradually adding more individuals as they progress from stage I to stage III, normally over a period of years, and normally involve drug companies, the government and its laboratories, and often medical schools and hospitals and clinics. However, any exceptions to the aforementioned process are subject to strict review and scrutiny and conditions, and are only given if a substantial amount of research and at least some preliminary human testing has shown that they are believed to be somewhat safe and possibly effective. (See FDA Special Protocol Assessment about Phase III trials.)

{{more citations needed section|date=August 2019}}

The FDA's Office of Prescription Drug Promotion (OPDP) has responsibilities that revolve around the review and regulation of prescription drug advertising and promotion. This is achieved through surveillance activities and the issuance of enforcement letters to pharmaceutical manufacturers.{{Cite web | work = Center for Drug Evaluation and Research |date=October 19, 2023 |title=The Office of Prescription Drug Promotion (OPDP) |url=https://www.fda.gov/about-fda/center-drug-evaluation-and-research-cder/office-prescription-drug-promotion-opdp |access-date=October 23, 2023 | publisher = U.S. Food and Drug Administration |language=en |archive-date=October 23, 2023 |archive-url=https://web.archive.org/web/20231023220954/https://www.fda.gov/about-fda/center-drug-evaluation-and-research-cder/office-prescription-drug-promotion-opdp |url-status=dead }} Advertising and promotion for over-the-counter drugs is regulated by the Federal Trade Commission. The FDA also implements regulatory oversight through engagement with third-party enforcer-firms. It expects pharmaceutical companies to ensure that third-party suppliers and labs comply with the agency's health and safety guidelines .{{Cite journal | vauthors = Van Loo R |date=April 1, 2020 |title=The New Gatekeepers: Private Firms as Public Enforcers |url=https://scholarship.law.bu.edu/faculty_scholarship/800 |journal=Virginia Law Review |volume=106 |issue=2 |page=467 |access-date=October 25, 2020 |archive-date=October 28, 2020 |archive-url=https://web.archive.org/web/20201028034638/https://scholarship.law.bu.edu/faculty_scholarship/800/ |url-status=live}}{{rp|4}}

The drug advertising regulation21 CFR 202: Prescription Drug Advertising. contains two broad requirements: (1) a company may advertise or promote a drug only for the specific indication or medical use for which it was approved by FDA. Also, an advertisement must contain a "fair balance" between the benefits and the risks (side effects) of a drug. The regulation of drug advertising in the U.S. is divided between the Food and Drug Administration (FDA) and the Federal Trade Commission (FTC), based on whether the drug in question is a prescription drug or an over-the-counter (OTC) drug. The FDA oversees the advertising of prescription drugs, while the FTC regulates the advertising of OTC drugs.{{cite journal | vauthors = Weinmeyer R | title = Direct-to-consumer advertising of drugs | journal = The Virtual Mentor | volume = 15 | issue = 11 | pages = 954–958 | date = November 2013 | pmid = 24257087 | doi = 10.1001/virtualmentor.2013.15.11.hlaw1-1311 | url = https://journalofethics.ama-assn.org/article/direct-consumer-advertising-drugs/2013-11 | url-status = live | archive-url = https://web.archive.org/web/20240131130241/https://journalofethics.ama-assn.org/article/direct-consumer-advertising-drugs/2013-11 | archive-date = January 31, 2024 | doi-access = free }}

The term off-label refers to the practice of prescribing a drug for a different purpose than what the FDA approved.{{Cite web |date=January 1, 2014 |title=Off-Label Drug Use in Cancer Treatment |url=https://www.cancer.gov/about-cancer/treatment/drugs/off-label |access-date=January 14, 2023 |website=NCI |language=en |archive-date=January 14, 2023 |archive-url=https://web.archive.org/web/20230114030805/https://www.cancer.gov/about-cancer/treatment/drugs/off-label |url-status=live }}

Due to this approval requirement, manufacturers were prohibited from advertising COVID-19 vaccines during the period in which they had only been approved under Emergency Use Authorization.{{Cite web |title=FDA rules have blocked COVID-19 vaccine makers from advertising on TV |url=https://www.tampabay.com/news/health/2021/10/25/fda-rules-have-blocked-covid-19-vaccine-makers-from-advertising-on-tv/ |website=Tampa Bay Times |access-date=September 27, 2024 |language=en |quote=Food and Drug Administration rules prohibit advertising of drugs that have not been fully approved by the FDA}}

After NDA approval, the sponsor must then review and report to the FDA every single patient adverse drug experience it learns of. They must report unexpected serious and fatal adverse drug events within 15 days, and other events on a quarterly basis.21 CFR 314.80: Postmarketing Reporting of Adverse Drug Experiences The FDA also receives directly adverse drug event reports through its MedWatch program.{{cite web | url = https://www.fda.gov/safety/medwatch-fda-safety-information-and-adverse-event-reporting-program | title = MedWatch: The FDA Safety Information and Adverse Event Reporting Program | archive-url = https://web.archive.org/web/20190422112808/https://www.fda.gov/Safety/MedWatch/default.htm | archive-date=April 22, 2019 | access-date = October 9, 2007 | url-status = live | publisher = U.S. Food and Drug Administration }} These reports are called "spontaneous reports" because reporting by consumers and health professionals is voluntary.

While this remains the primary tool of post-market safety surveillance, FDA requirements for post-marketing risk management are increasing. As a condition of approval, a sponsor may be required to conduct additional clinical trials, called Phase IV trials. In some cases, the FDA requires risk management plans called Risk Evaluation and Mitigation Strategies (REMS) for some drugs that require actions to be taken to ensure that the drug is used safely.{{cite journal | vauthors = Nelson LS, Loh M, Perrone J | title = Assuring safety of inherently unsafe medications: the FDA risk evaluation and mitigation strategies | journal = Journal of Medical Toxicology | volume = 10 | issue = 2 | pages = 165–172 | date = June 2014 | pmid = 24414251 | pmc = 4057549 | doi = 10.1007/s13181-013-0374-z }}{{cite journal | vauthors = Brown WV, Bramlet DA, Ross JL, Underberg JA | title = JCL roundtable: Risk evaluation and mitigation strategy | journal = Journal of Clinical Lipidology | volume = 10 | issue = 6 | pages = 1288–1296 | date = October 14, 2016 | pmid = 27919344 | doi = 10.1016/j.jacl.2016.10.007 }} For example, thalidomide can cause birth defects, but has uses that outweigh the risks if men and women taking the drugs do not conceive a child; a REMS program for thalidomide mandates an auditable process to ensure that people taking the drug take action to avoid pregnancy; many opioid drugs have REMS programs to avoid addiction and diversion of drugs. The drug isotretinoin has a REMS program called iPLEDGE.{{cite journal | vauthors = Kovitwanichkanont T, Driscoll T | title = A comparative review of the isotretinoin pregnancy risk management programs across four continents | journal = International Journal of Dermatology | volume = 57 | issue = 9 | pages = 1035–1046 | date = September 2018 | pmid = 29508918 | doi = 10.1111/ijd.13950 | s2cid = 3726217 }}

Generic drugs are chemical and therapeutic equivalents of name-brand drugs, normally whose patents have expired. Approved generic drugs should have the same dosage, safety, effectiveness, strength, stability, and quality, as well as route of administration. In general, they are less expensive than their name brand counterparts, are manufactured and marketed by rival companies and, in the 1990s, accounted for about a third of all prescriptions written in the United States. For a pharmaceutical company to gain approval to produce a generic drug, the FDA requires scientific evidence that the generic drug is interchangeable with or therapeutically equivalent to the originally approved drug.{{cite web |url=https://www.fda.gov/Drugs/DevelopmentApprovalProcess/HowDrugsareDevelopedandApproved/ApprovalApplications/AbbreviatedNewDrugApplicationANDAGenerics/ucm073182.htm |title=Therapeutic Equivalence of Generic Drugs |access-date=August 30, 2012 |publisher=Food and Drug Administration |year=1998 |archive-date=April 29, 2012 |archive-url=https://web.archive.org/web/20120429002732/http://www.fda.gov/Drugs/DevelopmentApprovalProcess/HowDrugsareDevelopedandApproved/ApprovalApplications/AbbreviatedNewDrugApplicationANDAGenerics/ucm073182.htm |url-status=dead}} This is called an Abbreviated New Drug Application (ANDA).{{cite web |title=Abbreviated New Drug Application (ANDA) |date=December 20, 2019 |publisher=U.S. Food & Drug Administration |url=https://www.fda.gov/drugs/types-applications/abbreviated-new-drug-application-anda |access-date=May 10, 2020 |archive-date=September 23, 2020 |archive-url=https://web.archive.org/web/20200923221401/https://www.fda.gov/drugs/types-applications/abbreviated-new-drug-application-anda |url-status=dead}} 80% of prescription drugs sold in the United States are generic brands.{{cite web | vauthors = Saling J | title=Generic Drugs: Answers to Common Questions | website=WebMD | date=March 5, 2024 | url=https://www.webmd.com/healthy-aging/generic-drugs-answers-to-common-questions | access-date=May 27, 2024 |quote=Almost 80% of prescription drugs sold are generics.}}

In 1989, a major scandal erupted involving the procedures used by the FDA to approve generic drugs for sale to the public.{{cite encyclopedia | vauthors = Cohen L |article=Government Policies and Programs – United States – Generic Drug Scandal |title=The New Book of Knowledge – Medicine And Health |date=1990 |pages=276–281 |isbn=978-0-7172-8244-9}} Charges of corruption in generic drug approval first emerged in 1988 during the course of an extensive congressional investigation into the FDA. The oversight subcommittee of the United States House Energy and Commerce Committee resulted from a complaint brought against the FDA by Mylan Laboratories Inc. of Pittsburgh. When its application to manufacture generics were subjected to repeated delays by the FDA, Mylan, convinced that it was being discriminated against, soon began its own private investigation of the agency in 1987. Mylan eventually filed suit against two former FDA employees and four drug-manufacturing companies, charging that corruption within the federal agency resulted in racketeering and in violations of antitrust law. "The order in which new generic drugs were approved was set by the FDA employees even before drug manufacturers submitted applications" and, according to Mylan, this illegal procedure was followed to give preferential treatment to certain companies. During the summer of 1989, three FDA officials (Charles Y. Chang, David J. Brancato, Walter Kletch) pleaded guilty to criminal charges of accepting bribes from generic drugs makers, and two companies (Par Pharmaceutical and its subsidiary Quad Pharmaceuticals){{cite news |url=https://www.nytimes.com/1989/09/12/business/fda-details-problems-at-drug-makers.html |work=The New York Times |title=F.D.A. Details Problems at Drug Makers |date=September 12, 1989 |access-date=February 7, 2017 |archive-date=March 13, 2017 |archive-url=https://web.archive.org/web/20170313215132/http://www.nytimes.com/1989/09/12/business/fda-details-problems-at-drug-makers.html |url-status=live}} pleaded guilty to giving bribes.

Furthermore, it was discovered that several manufacturers had falsified data submitted in seeking FDA authorization to market certain generic drugs. Vitarine Pharmaceuticals of New York, which sought approval of a generic version of the drug Dyazide, a medication for high blood pressure, submitted Dyazide, rather than its generic version, for the FDA tests. In April 1989, the FDA investigated 11 manufacturers for irregularities; and later brought that number up to 13. Dozens of drugs were eventually suspended or recalled by manufacturers. In the early 1990s, the U.S. Securities and Exchange Commission filed securities fraud charges against the Bolar Pharmaceutical Company, a major generic manufacturer based in Long Island, New York.

Over-the-counter (OTC) are drugs like aspirin that do not require a doctor's prescription.{{cite web | url = https://www.fda.gov/downloads/AboutFDA/CentersOffices/OfficeofMedicalProductsandTobacco/CDER/UCM148055.pdf | title = Regulation of Nonprescription Drug Products | publisher = U.S. Food and Drug Administration | archive-url = https://web.archive.org/web/20180226021613/https://www.fda.gov/downloads/AboutFDA/CentersOffices/OfficeofMedicalProductsandTobacco/CDER/UCM148055.pdf | archive-date=February 26, 2018 | access-date = August 30, 2012 }} The FDA has a list of approximately 800 such approved ingredients that are combined in various ways to create more than 100,000 OTC drug products. Many OTC drug ingredients had been previously approved prescription drugs now deemed safe enough for use without a medical practitioner's supervision like ibuprofen.{{cite web |url=https://www.fda.gov/cder/handbook/otcintro.htm |title=FDA CDER Handbook: Over-the-Counter Drug Products |website=Food and Drug Administration |access-date=October 9, 2007 |archive-date=May 12, 2009 |archive-url=https://web.archive.org/web/20090512224542/https://www.fda.gov/cder/handbook/otcintro.htm}}

In 2014, the FDA added an Ebola treatment being developed by Canadian pharmaceutical company Tekmira to the Fast Track program, but halted the phase 1 trials in July pending the receipt of more information about how the drug works. This was widely viewed as increasingly important in the face of a major outbreak of the disease in West Africa that began in late March 2014 and ended in June 2016.{{cite web | vauthors = Kliff S |title=The FDA recently halted trials on a potential Ebola treatment |url=https://www.vox.com/2014/8/3/5962381/ebola-outbreak-vaccine-fda-halted-trials |website=Vox |access-date=August 4, 2014 |date=August 3, 2014 |archive-date=August 6, 2014 |archive-url=https://web.archive.org/web/20140806035748/http://www.vox.com/2014/8/3/5962381/ebola-outbreak-vaccine-fda-halted-trials |url-status=live}}

{{Main|COVID-19 testing}}

During the coronavirus pandemic, FDA granted emergency use authorization for personal protective equipment (PPE), in vitro diagnostic equipment, ventilators and other medical devices.{{cite web |url=https://www.fda.gov/medical-devices/emergency-situations-medical-devices/emergency-use-authorizations-medical-devices |title=Emergency Use Authorizations - FDA |author= |date=May 21, 2020 | publisher = U.S. Food and Drug Administration |access-date=May 21, 2020 |url-status=live |archive-url=https://web.archive.org/web/20200517205323/https://www.fda.gov/medical-devices/emergency-situations-medical-devices/emergency-use-authorizations |archive-date=May 17, 2020}}{{cite journal | vauthors = Rizk JG, Forthal DN, Kalantar-Zadeh K, Mehra MR, Lavie CJ, Rizk Y, Pfeiffer JP, Lewin JC | title = Expanded Access Programs, compassionate drug use, and Emergency Use Authorizations during the COVID-19 pandemic | journal = Drug Discovery Today | volume = 26 | issue = 2 | pages = 593–603 | date = February 2021 | pmid = 33253920 | pmc = 7694556 | doi = 10.1016/j.drudis.2020.11.025 }}{{Cite journal |url=https://www.fda.gov/media/144413/download |title=Comirnaty and Pfizer-BioNTech COVID-19 Vaccine |journal=FDA |date=January 3, 2022 |access-date=October 27, 2021 |archive-date=August 14, 2021 |archive-url=https://web.archive.org/web/20210814042307/https://www.fda.gov/media/144413/download |url-status=dead }}

On March 18, 2020, FDA inspectors postponed most foreign facility inspections and all domestic routine surveillance facility inspections.{{cite web |url=https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-focuses-safety-regulated-products-while-scaling-back-domestic |title=Coronavirus (COVID-19) Update: FDA Focuses on Safety of Regulated Products While Scaling Back Domestic Inspections |author=Stephen M. Hahn M.D., Commissioner of Food and Drugs - Food and Drug Administration |date=March 18, 2020 |publisher=U.S. Food and Drug Administration |access-date=May 21, 2020 |url-status=dead |archive-url=https://web.archive.org/web/20200512170315/https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-focuses-safety-regulated-products-while-scaling-back-domestic |archive-date=May 12, 2020 |quote=Earlier this month, we announced that we are postponing most foreign facility inspections through April and that inspections outside the U.S. deemed mission-critical will be considered on a case-by-case basis as this outbreak continues to unfold. Today, we're announcing that for the health and well-being of our staff and those who conduct inspections for the agency under contract at the state level, and because of industry concerns about visitors, we have temporarily postponed all domestic routine surveillance facility inspections. These are facility inspections the FDA traditionally conducts every few years based on a risk analysis. Importantly, all domestic for-cause inspection assignments will be evaluated and will proceed if mission-critical. We will continue to respond to natural disasters, outbreaks and other public health emergencies involving FDA-regulated products.}} In contrast, the USDA's Food Safety and Inspection Service (FSIS) continued inspections of meatpacking plants, which resulted in 145 FSIS field employees who tested positive for COVID-19, and three who died.{{cite news | vauthors = Carney J |date=May 5, 2020 |title=3 USDA meat inspectors dead, about 145 diagnosed with COVID-19 |url=https://www.cbsnews.com/news/coronavirus-usda-meat-inspectors-3-dead-covid-19/ |url-status=live |work=CBS News |archive-url=https://web.archive.org/web/20200519054805/https://www.cbsnews.com/news/coronavirus-usda-meat-inspectors-3-dead-covid-19/ |archive-date=May 19, 2020 |access-date=May 22, 2020}}

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File:Blood Research- Saving Lives (8352) (9759352093).jpg

The Center for Biologics Evaluation and Research is the branch of the FDA responsible for ensuring the safety and efficacy of biological therapeutic agents.{{cite web |url=https://www.fda.gov/AboutFDA/CentersOffices/OfficeofMedicalProductsandTobacco/CBER/ |title=About the Center for Biologics Evaluation and Research (CBER) |publisher=Food and Drug Administration |date=March 2, 2017 |access-date=May 12, 2017 |archive-date=May 9, 2017 |archive-url=https://web.archive.org/web/20170509063921/https://www.fda.gov/AboutFDA/CentersOffices/OfficeofMedicalProductsandTobacco/CBER/ |url-status=dead}}.{{Cite web |title=Center for Biologics Evaluation and Research |url=https://registries.ncats.nih.gov/glossary/center-for-biologics-evaluation-and-research/ |access-date=January 2, 2025 |website=RaDaR |language=en-US}} These include blood and blood products, vaccines, allergenics, cell and tissue-based products, and gene therapy products. New biologics are required to go through a premarket approval process called a Biologics License Application (BLA), similar to that for drugs.

The original authority for government regulation of biological products was established by the 1902 Biologics Control Act, with additional authority established by the 1944 Public Health Service Act. Along with these Acts, the Federal Food, Drug, and Cosmetic Act applies to all biologic products, as well. Originally, the entity responsible for regulation of biological products resided under the National Institutes of Health; this authority was transferred to the FDA in 1972.

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The Center for Devices and Radiological Health (CDRH) is the branch of the FDA responsible for the premarket approval of all medical devices, as well as overseeing the manufacturing, performance and safety of these devices.{{cite web | url = https://www.fda.gov/AboutFDA/CentersOffices/OfficeofMedicalProductsandTobacco/CDRH/ucm300639.htm | title = CDRH Mission, Vision and Shared Values | archive-url = https://web.archive.org/web/20190422142129/https://www.fda.gov/AboutFDA/CentersOffices/OfficeofMedicalProductsandTobacco/CDRH/ucm300639.htm | archive-date=April 22, 2019 | access-date = August 30, 2012 | publisher = U.S. Food and Drug Administration }} The definition of a medical device is given in the FD&C Act, and it includes products from the simple toothbrush to complex devices such as implantable neurostimulators. CDRH also oversees the safety performance of non-medical devices that emit certain types of electromagnetic radiation. Examples of CDRH-regulated devices include cellular phones, airport baggage screening equipment, television receivers, microwave ovens, tanning booths, and laser products.{{Cite web |date=June 13, 2022 |title=FDA Center for Devices and Radiological Health (CDRH) - NCI |url=https://sbir.cancer.gov/commercialization/fda/radiological-devices |access-date=January 2, 2025 |website=sbir.cancer.gov |language=en}}

CDRH regulatory powers include the authority to require certain technical reports from the manufacturers or importers of regulated products, to require that radiation-emitting products meet mandatory safety performance standards, to declare regulated products defective, and to order the recall of defective or noncompliant products. CDRH also conducts limited amounts of direct product testing.

Clearance requests are required for medical devices that prove they are "substantially equivalent" to the predicate devices already on the market. Approved requests are for items that are new or substantially different and need to demonstrate "safety and efficacy", for example they may be inspected for safety in case of new toxic hazards. Both aspects need to be proved or provided by the submitter to ensure proper procedures are followed.{{cite web |url=https://www.fda.gov/AboutFDA/Transparency/Basics/ucm194460.htm |title=What does it mean when FDA "clears" or "approves" a medical device? |publisher=Food and Drug Administration |access-date=March 14, 2015 |archive-date=March 7, 2015 |archive-url=https://web.archive.org/web/20150307000034/http://www.fda.gov/AboutFDA/Transparency/Basics/ucm194460.htm |url-status=dead}}

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Cosmetics are regulated by the Center for Food Safety and Applied Nutrition, the same branch of the FDA that regulates food. Cosmetic products are not, in general, subject to premarket approval by the FDA unless they make "structure or function claims" that make them into drugs (see Cosmeceutical). However, all color additives must be specifically FDA approved before manufacturers can include them in cosmetic products sold in the U.S. The FDA regulates cosmetics labeling, and cosmetics that have not been safety tested must bear a warning to that effect.{{Cite web |url=https://www.fda.gov/cosmetics/cosmetics-labeling-regulations/summary-cosmetics-labeling-requirements |title=Summary of Cosmetics Labeling Requirements |date=August 2, 2018 |website=U.S. Food and Drug Administration |access-date=December 4, 2019 |archive-date=December 13, 2019 |archive-url=https://web.archive.org/web/20191213121829/https://www.fda.gov/cosmetics/cosmetics-labeling-regulations/summary-cosmetics-labeling-requirements |url-status=live}}

According to the industry advocacy group, the American Council on Science and Health, though the cosmetic industry is primarily responsible for its own product safety, the FDA can intervene when necessary to protect the public. In general, though, cosmetics do not require pre-market approval or testing. The ACSH says that companies must place a warning note on their products if they have not been tested, and that experts in cosmetic ingredient review also play a role in monitoring safety through influence on ingredients, but they lack legal authority. According to the ACSH, it has reviewed about 1,200 ingredients and has suggested that several hundred be restricted—but there is no standard or systemic method for reviewing chemicals for safety, or a clear definition of what 'safety' even means so that all chemicals get tested on the same basis.{{cite journal | vauthors = Ross G | title = A perspective on the safety of cosmetic products: a position paper of the American Council on Science and Health | journal = International Journal of Toxicology | volume = 25 | issue = 4 | pages = 269–277 | year = 2006 | pmid = 16815815 | doi = 10.1080/10915810600746049 | s2cid = 21904805 | doi-access = free }}

However, on December 29, 2022, President Biden signed the '2023 Consolidated Budget Act',{{Cite web |title=Biden signs $1.7T government spending bill, ensuring funding for most of 2023 |url=https://abcnews.go.com/Politics/biden-signs-17t-government-spending-bill-ensuring-funding/story?id=95934378 |access-date=January 2, 2025 |website=ABC News |language=en}} which includes the 'Cosmetics Regulatory Modernization Act of 2022 (MoCRA)', which is a stricter regulation that is different from the previous regulations. MoCRA requires compliance with matters such as serious adverse event reporting, safety substantiation, additional labeling, record keeping, and Good Manufacturing Practices (GMP).{{Cite web |title=MoCRA Cosmetic Testing and Certification |url=https://www.nsf.org/au/en/knowledge-library/fda-modernization-cosmetics-regulation-act |access-date=January 2, 2025 |website=www.nsf.org |language=en}} MoCRA also calls on the FDA to grant Mandatory Recall Authority and establish regulations for GMP rules, flavor allergen labeling rules, and testing methods for cosmetics containing talc.{{cite web |title=Modernization of Cosmetics Regulation Act of 2022 (MoCRA) |url=https://www.fda.gov/cosmetics/cosmetics-laws-regulations/modernization-cosmetics-regulation-act-2022-mocra#:~:text=Mandatory%20Recall%20Authority%3A%20If%20the,if%20the%20responsible%20person%20refuses | publisher = U.S. Food and Drug Administration |date=December 14, 2023 |access-date=January 21, 2024 |archive-date=January 22, 2024 |archive-url=https://web.archive.org/web/20240122175633/https://www.fda.gov/cosmetics/cosmetics-laws-regulations/modernization-cosmetics-regulation-act-2022-mocra#:~:text=Mandatory%20Recall%20Authority%3A%20If%20the,if%20the%20responsible%20person%20refuses |url-status=dead }}

The Center for Veterinary Medicine (CVM) is a center of the FDA that regulates food additives and drugs that are given to animals.{{cite journal | vauthors = Modric S | title = Regulatory framework for the availability and use of animal drugs in the United States | journal = The Veterinary Clinics of North America. Small Animal Practice | volume = 43 | issue = 5 | pages = 1005–1012 | date = September 2013 | pmid = 23890234 | doi = 10.1016/j.cvsm.2013.04.001 }} CVM regulates animal drugs, animal food including pet animal, and animal medical devices. The FDA's requirements to prevent the spread of bovine spongiform encephalopathy are also administered by CVM through inspections of feed manufacturers.{{Cite web |url=https://www.fda.gov/animal-veterinary/compliance-enforcement/bovine-spongiform-encephalopathy |title=Bovine Spongiform Encephalopathy | work = Center for Veterinary Medicine |date=April 11, 2019 | publisher = U.S. Food and Drug Administ ration |language=en |access-date=February 4, 2020 |archive-date=December 12, 2019 |archive-url=https://web.archive.org/web/20191212171837/https://www.fda.gov/animal-veterinary/compliance-enforcement/bovine-spongiform-encephalopathy |url-status=live}} CVM does not regulate vaccines for animals; these are handled by the United States Department of Agriculture.{{cite book | vauthors = Hill R Jr, Foley P, Clough N, Ludemann L, Murtle D | veditors = Roth J, Richt J, Morozov I |title=Vaccines and diagnostics for transboundary animal diseases: Ames, Iowa, 17-19 September 2012 |date=2013 |publisher=Karger Medical and Scientific Publishers |isbn=978-3-318-02366-4 |pages=53–54 |chapter-url=https://books.google.com/books?id=wZ86AQAAQBAJ&pg=PA53 |chapter=Translating research into licensed vaccines and validated and licensed diagnostic tests |access-date=June 30, 2019 |archive-date=August 1, 2020 |archive-url=https://web.archive.org/web/20200801131751/https://books.google.com/books?id=wZ86AQAAQBAJ&pg=PA53 |url-status=live}}

The FDA regulates tobacco products with authority established by the 2009 Family Smoking Prevention and Tobacco Control Act.{{cite web |url=https://www.fda.gov/AboutFDA/Transparency/Basics/ucm194423.htm |title=Does FDA have the authority to regulate tobacco products? |publisher=Food and Drug Administration |access-date=December 16, 2019 |archive-date=November 14, 2017 |archive-url=https://web.archive.org/web/20171114204636/https://www.fda.gov/AboutFDA/Transparency/Basics/ucm194423.htm |url-status=dead}} This Act requires color warnings on cigarette packages and printed advertising, and text warnings from the U.S. Surgeon General.{{cite news |url=https://www.foxnews.com/health/cigarette-makers-fda-clash-over-new-graphic-ads/ |work=Fox News |title=Cigarette Makers, FDA Clash Over New Graphic Ads |date=September 22, 2011 |access-date=October 13, 2011 |archive-date=October 8, 2011 |archive-url=https://web.archive.org/web/20111008214526/http://www.foxnews.com/health/2011/09/22/cigarette-makers-fda-clash-over-new-graphic-ads/ |url-status=live}}

The nine new graphic warning labels were announced by the FDA in June 2011 and were scheduled to be required to appear on packaging by September 2012. The implementation date is uncertain, due to ongoing proceedings in the case of R.J. Reynolds Tobacco Co. v. U.S. Food and Drug Administration.{{cite web |url=https://www.fda.gov/TobaccoProducts/Labeling/ucm259214.htm |publisher=Food and Drug Administration |title=Overview: Cigarette Health Warnings |access-date=August 30, 2012 |archive-date=September 9, 2012 |archive-url=https://web.archive.org/web/20120909034823/http://www.fda.gov/TobaccoProducts/Labeling/ucm259214.htm |url-status=dead}} R.J. Reynolds, Lorillard, Commonwealth Brands, Liggett Group and Santa Fe Natural Tobacco Company have filed suit in Washington, D.C. federal court claiming that the graphic labels are an unconstitutional way of forcing tobacco companies to engage in anti-smoking advocacy on the government's behalf.{{cite news |url=https://blogs.wsj.com/law/2011/09/12/fda-defends-new-graphic-cigarette-labels/ |work=The Wall Street Journal | vauthors = Koppel N |title=FDA Defends New Graphic Cigarette Labels |date=September 12, 2011 |url-access=subscription |access-date=August 4, 2017 |archive-date=July 9, 2017 |archive-url=https://web.archive.org/web/20170709181720/https://blogs.wsj.com/law/2011/09/12/fda-defends-new-graphic-cigarette-labels/ |url-status=live}}

A First Amendment lawyer, Floyd Abrams, is representing the tobacco companies in the case, contending requiring graphic warning labels on a lawful product cannot withstand constitutional scrutiny.{{cite web |url=http://www.adweek.com/news/advertising-branding/big-tobacco-gets-top-first-amendment-lawyer-new-suit-134200 |title=Big Tobacco Gets Top First Amendment Lawyer for New Suit |work=AdWeek |date=August 18, 2011 |access-date=March 14, 2015 |archive-date=April 11, 2015 |archive-url=https://web.archive.org/web/20150411073933/http://www.adweek.com/news/advertising-branding/big-tobacco-gets-top-first-amendment-lawyer-new-suit-134200 |url-status=live}} The Association of National Advertisers and the American Advertising Federation have also filed a brief in the suit, arguing that the labels infringe on commercial free speech and could lead to further government intrusion if left unchallenged.{{cite web |url=http://www.csnews.com/product-categories/tobacco/tobacco-cos-get-allies-warning-label-fight |title=Tobacco Cos. Get Allies in Warning Label Fight |work=Convenience Store News |date=September 19, 2011 |access-date=March 14, 2015 |archive-date=January 12, 2015 |archive-url=https://web.archive.org/web/20150112022328/http://www.csnews.com/product-categories/tobacco/tobacco-cos-get-allies-warning-label-fight |url-status=live}} In November 2011, Federal judge Richard Leon of the U.S. District Court for the District of Columbia temporarily halted the new labels, likely delaying the requirement that tobacco companies display the labels. The U.S. Supreme Court ultimately could decide the matter.{{cite news |url=https://www.wsj.com/articles/SB10001424052970204554204577024040240467970 |work=The Wall Street Journal | vauthors = Esterl M |title=Judge Temporarily Blocks Graphic Cigarette Labels |date=November 8, 2011 |url-access=subscription |access-date=August 3, 2017 |archive-date=July 9, 2017 |archive-url=https://web.archive.org/web/20170709173439/https://www.wsj.com/articles/SB10001424052970204554204577024040240467970 |url-status=live}}

In July 2017, the FDA announced a plan that would reduce the current levels of nicotine permitted in tobacco cigarettes.{{cite web |url=https://www.npr.org/2017/07/28/540088353/fda-announces-plan-to-cut-level-of-nicotine-allowed-in-cigarettes |title=FDA Announces Plan To Cut Level Of Nicotine Allowed In Cigarettes |website=NPR |access-date=April 4, 2018 |archive-date=March 20, 2018 |archive-url=https://web.archive.org/web/20180320032301/https://www.npr.org/2017/07/28/540088353/fda-announces-plan-to-cut-level-of-nicotine-allowed-in-cigarettes |url-status=live}} The proposed regulation, identified as RIN 0910-AI76, titled "Tobacco Product Standard for Nicotine Yield of Cigarettes and Certain Other Combusted Tobacco Products," seeks to reduce the nicotine content in cigarettes to approximately 0.7 milligrams per gram of tobacco.

With acceptance of premarket notification 510(k) k033391 in January 2004,{{cite web |title=510(k) Premarket Notification K033391 |url=https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm?ID=K033391 |publisher=FDA |access-date=July 4, 2021 |archive-date=July 9, 2021 |archive-url=https://web.archive.org/web/20210709184153/https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm?ID=K033391 |url-status=dead }} the FDA granted Ronald Sherman permission to produce and market medical maggots for use in humans or other animals as a prescription medical device.{{cite web |title=FDA_K033391_ClearanceLetter |url=https://www.accessdata.fda.gov/cdrh_docs/pdf3/K033391.pdf |archive-url=https://web.archive.org/web/20150701125329/http://www.accessdata.fda.gov/cdrh_docs/pdf3/K033391.pdf |archive-date=July 1, 2015 |url-status=dead |publisher=FDA |access-date=July 4, 2021}} Medical maggots represent the first living organism allowed by the Food and Drug Administration for production and marketing as a prescription medical device.{{cite journal | vauthors = Sherman R | title = Age-old therapy gets new approval | journal = Advances in Skin & Wound Care | volume = 18 | issue = 1 | pages = 12–15 | date = 2005 | pmid = 15716781 | doi = 10.1097/00129334-200501000-00003 | doi-access = free }}

In June 2004, the FDA cleared Hirudo medicinalis (medicinal leeches) as the second living organism legal to use as a medical device.{{Cite web |title=FDA approves leeches as medical devices |url=http://www.nbcnews.com/health/health-news/fda-approves-leeches-medical-devices-flna1C9447212 |access-date=January 14, 2023 |website=NBC News |date=June 28, 2004 |language=en |archive-date=January 14, 2023 |archive-url=https://web.archive.org/web/20230114031405/https://www.nbcnews.com/health/health-news/fda-approves-leeches-medical-devices-flna1C9447212 |url-status=live }}

The FDA also requires that milk be pasteurized to remove bacteria.{{Cite journal |date=January 26, 2022 |title=The Dangers of Raw Milk: Unpasteurized Milk Can Pose a Serious Health Risk |url=https://www.fda.gov/food/buy-store-serve-safe-food/dangers-raw-milk-unpasteurized-milk-can-pose-serious-health-risk |journal=FDA |language=en |access-date=January 14, 2023 |archive-date=April 4, 2021 |archive-url=https://web.archive.org/web/20210404003528/https://www.fda.gov/food/buy-store-serve-safe-food/dangers-raw-milk-unpasteurized-milk-can-pose-serious-health-risk |url-status=live }}

In February 2011, President Barack Obama and Canadian Prime Minister Stephen Harper issued a "Declaration on a Shared Vision for Perimeter Security and Economic Competitiveness"{{cite press release |url=https://obamawhitehouse.archives.gov/the-press-office/2011/02/04/joint-statement-president-obama-and-prime-minister-harper-canada-regul-0 |title=Joint Statement by President Obama and Prime Minister Harper of Canada on Regulatory Cooperation |date=February 4, 2011 |access-date=February 26, 2011 |archive-date=January 22, 2017 |archive-url=https://web.archive.org/web/20170122200817/https://obamawhitehouse.archives.gov/the-press-office/2011/02/04/joint-statement-president-obama-and-prime-minister-harper-canada-regul-0 |via=National Archives |work=whitehouse.gov |url-status=live}}{{cite press release |url=http://www.pm.gc.ca/eng/media.asp?id=3931 |title=PM and U.S. President Obama announce shared vision for perimeter security and economic competitiveness between Canada and the United States |publisher=Prime Minister of Canada |date=February 4, 2011 |access-date=February 26, 2011 |archive-url=https://web.archive.org/web/20110219142120/http://www.pm.gc.ca/eng/media.asp?id=3931 |archive-date=February 19, 2011}} and announced the creation of the Canada-United States Regulatory Cooperation Council (RCC) "to increase regulatory transparency and coordination between the two countries."{{cite press release |date=December 7, 2011 |url=http://pm.gc.ca/eng/media.asp?id=4511 |publisher=Office of the Prime Minister of Canada |title=United States-Canada Regulatory Cooperation Council (RCC) Joint Action Plan: Developing and implementing the Joint Action Plan |archive-url=https://web.archive.org/web/20130729152814/http://pm.gc.ca/eng/media.asp?id=4511 |archive-date=July 29, 2013}}

Under the RCC mandate, the FDA and Health Canada undertook a "first of its kind" initiative by selecting "as its first area of alignment common cold indications for certain over-the-counter antihistamine ingredients (GC 2013-01-10)."{{cite web |publisher=Government of Canada |series=Canada's Action Plan |title=Notice: Regulatory Cooperation Council (RCC) Over-the-Counter (OTC) Products: Common Monograph Working Group: Selection of a Monograph for Alignment |url=http://actionplan.gc.ca/en/page/rcc-ccr/notice-regulatory-cooperation-council-rcc-over |date=January 10, 2013 |access-date=February 15, 2013 |archive-url=https://web.archive.org/web/20141108070216/http://actionplan.gc.ca/en/page/rcc-ccr/notice-regulatory-cooperation-council-rcc-over |archive-date=November 8, 2014}}

A more recent example of the FDA's international work is their 2018 cooperation with regulatory and law-enforcement agencies worldwide through Interpol as part of Operation Pangea XI.{{Cite web |url=https://www.interpol.int/News-and-media/News/2018/N2018-123 |title=N2018-123 / 2018 / News / News and media / Internet / Home - INTERPOL |website=Interpol.int |access-date=February 8, 2019 |archive-date=February 9, 2019 |archive-url=https://web.archive.org/web/20190209123957/https://www.interpol.int/News-and-media/News/2018/N2018-123}}{{Cite web |url=https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm624070.htm |title=Press Announcements - FDA launches global operation to crack down on websites selling illegal, potentially dangerous drugs; including opioids | author = Office of the Commissioner |publisher=Food and Drug Administration |access-date=February 8, 2019 |archive-date=February 7, 2019 |archive-url=https://web.archive.org/web/20190207132558/https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm624070.htm |url-status=dead}} The FDA targeted 465 websites that illegally sold potentially dangerous, unapproved versions of opioid, oncology, and antiviral prescription drugs to U.S. consumers. The agency focused on transaction laundering schemes in order to uncover the complex online drug network.{{Cite web |url=https://www.thepaypers.com/expert-opinion/transaction-laundering-in-2019-time-to-review-the-monitoring-strategy/776727 |title=Transaction laundering in 2019 – time to review the monitoring strategy |publisher=The Paypers |access-date=February 8, 2019 |archive-date=July 14, 2020 |archive-url=https://web.archive.org/web/20200714025734/https://thepaypers.com/expert-opinion/transaction-laundering-in-2019-time-to-review-the-monitoring-strategy/776727 |url-status=live}}

File:FDA Bldg 64 - Lab (5160771733).jpg

The FDA carries out research and development activities to develop technology and standards that support its regulatory role, with the objective of resolving scientific and technical challenges before they become impediments. The FDA's research efforts include the areas of biologics, medical devices, drugs, women's health, toxicology, food safety and applied nutrition, and veterinary medicine.{{cite web |title=About Science & Research at FDA |url=https://www.fda.gov/ScienceResearch/AboutScienceResearchatFDA/ |publisher=Food and Drug Administration |access-date=November 25, 2011 |date=June 18, 2009 |archive-date=January 14, 2012 |archive-url=https://web.archive.org/web/20120114151200/http://www.fda.gov/ScienceResearch/AboutScienceResearchatFDA/ |url-status=dead}}

The FDA has collected a large amount of data through the decades. The OpenFDA project was created to enable easy access of the data for the public and was officially launched in June 2014.{{Cite web |date=September 11, 2019 |title=openFDA |url=https://www.fda.gov/science-research/health-informatics-fda/openfda |access-date=October 3, 2020 |website=U.S. Food and Drug Administration |archive-date=October 21, 2020 |archive-url=https://web.archive.org/web/20201021204036/https://www.fda.gov/science-research/health-informatics-fda/openfda |url-status=dead}}{{Cite news |date=June 7, 2014 |title=FDA opens new drug database to public; hiring site draws investor interest |newspaper=Washington Post |url=https://www.washingtonpost.com/business/economy/fda-opens-new-drug-database-to-public-hiring-site-draws-investor-interest/2014/06/07/624fcbaa-eb43-11e3-9f5c-9075d5508f0a_story.html |url-status=live |archive-date=June 23, 2014 |archive-url=https://web.archive.org/web/20140623084015/http://www.washingtonpost.com/business/economy/fda-opens-new-drug-database-to-public-hiring-site-draws-investor-interest/2014/06/07/624fcbaa-eb43-11e3-9f5c-9075d5508f0a_story.html}}

{{Main|History of the Food and Drug Administration}}

Up until the 20th century, there were few federal laws regulating the contents and sale of domestically produced food and pharmaceuticals, with one exception being the Vaccine Act of 1813.{{Cite book | author = ((National Research Council (US) Division of Health Promotion and Disease Prevention)) |url=https://www.ncbi.nlm.nih.gov/books/NBK216821/ |title=Vaccines: Past, Present, and Future |date=1985 |publisher=National Academies Press (US) |language=en |access-date=January 14, 2023 |archive-date=June 27, 2023 |archive-url=https://web.archive.org/web/20230627130317/http://www.ncbi.nlm.nih.gov/books/NBK216821/ |url-status=live }} The history of the FDA can be traced to the latter part of the 19th century and the Division of Chemistry of the U.S. Department of Agriculture,{{cite journal | vauthors = Swann JP |title=How Chemists Pushed for Consumer Protection: The Food and Drugs Act of 1906 |journal=Chemical Heritage |date=Summer 2006 |volume=24 |issue=2 |pages=6–11 |url=https://www.fda.gov/media/110307/download |access-date=September 17, 2021 |archive-date=September 17, 2021 |archive-url=https://web.archive.org/web/20210917071757/https://www.fda.gov/media/110307/download |url-status=live }} which itself derived from the Copyright and Patent Clause. Under Harvey Washington Wiley, appointed chief chemist in 1883, the Division began conducting research into the adulteration and misbranding of food and drugs on the American market. Wiley's advocacy came at a time when the public had become aroused to hazards in the marketplace by muckraking journalists like Upton Sinclair, and became part of a general trend for increased federal regulations in matters pertinent to public safety during the Progressive Era.{{cite web |url=https://www.fda.gov/AboutFDA/WhatWeDo/History/Origin/ucm054819.htm |title=FDA History — Part I |publisher=Food and Drug Administration |access-date=March 14, 2015 |archive-date=March 16, 2015 |archive-url=https://web.archive.org/web/20150316152305/http://www.fda.gov/AboutFDA/WhatWeDo/History/Origin/ucm054819.htm |url-status=dead}} The Biologics Control Act of 1902 was put in place after a diphtheria antitoxin derived from tetanus-contaminated serum caused the deaths of thirteen children in St. Louis, Missouri. The serum was originally collected from a horse named Jim who had contracted tetanus.{{Cite web |last=cirmweb |date=June 4, 2012 |title=The surprising journey from a horse named Jim to stem cell therapies at UC Davis |url=https://blog.cirm.ca.gov/2012/06/04/surprising-journey-from-horse-named-jim/ |access-date=January 14, 2023 |website=The Stem Cellar |language=en |archive-date=January 14, 2023 |archive-url=https://web.archive.org/web/20230114025520/https://blog.cirm.ca.gov/2012/06/04/surprising-journey-from-horse-named-jim/ |url-status=live }}

File:Portrait of Dr. Harvey W. Wiley (FDA 107) (8203830456).jpg, chief advocate of the Food and Drug Act]]

In June 1906, President Theodore Roosevelt signed into law the Pure Food and Drug Act of 1906, also known as the "Wiley Act" after its chief advocate. The Act prohibited, under penalty of seizure of goods, the interstate transport of food that had been "adulterated". The Act applied similar penalties to the interstate marketing of "adulterated" drugs, in which the "standard of strength, quality, or purity" of the active ingredient was not either stated clearly on the label or listed in the United States Pharmacopeia or the National Formulary.{{cite web |url=https://www.fda.gov/opacom/laws/wileyact.htm |title=Laws Enforced by FDA | author = Office of the Commissioner |publisher=Food and Drug Administration |access-date=December 16, 2019 |archive-date=May 12, 2009 |archive-url=https://web.archive.org/web/20090512143516/http://www.fda.gov/opacom/laws/wileyact.htm |url-status=dead}}

The responsibility for examining food and drugs for such "adulteration" or "misbranding" was given to Wiley's USDA Bureau of Chemistry. Wiley used these new regulatory powers to pursue an aggressive campaign against the manufacturers of foods with chemical additives, but the Chemistry Bureau's authority was soon checked by judicial decisions, which narrowly defined the bureau's powers and set high standards for proof of fraudulent intent. In 1927, the Bureau of Chemistry's regulatory powers were reorganized under a new USDA body, the Food, Drug, and Insecticide Administration.{{Cite web |date=March 14, 2019 |title=History of FDA's Internal Organization |url=https://www.fda.gov/about-fda/history-fdas-fight-consumer-protection-and-public-health/history-fdas-internal-organization |access-date=October 3, 2020 |website=U.S. Food and Drug Administration |language=en |archive-date=September 24, 2020 |archive-url=https://web.archive.org/web/20200924220535/https://www.fda.gov/about-fda/history-fdas-fight-consumer-protection-and-public-health/history-fdas-internal-organization |url-status=dead }} This name was shortened to the Food and Drug Administration (FDA) three years later.{{cite web |url=https://www.fda.gov/opacom/backgrounders/miles.html |title=Milestones in U.S. Food and Drug Law History |website=Food and Drug Administration |access-date=December 16, 2019 |archive-date=May 21, 2009 |archive-url=https://web.archive.org/web/20090521181634/http://www.fda.gov/opacom/backgrounders/miles.html |url-status=dead}}

By the 1930s, muckraking journalists, consumer protection organizations, and federal regulators began mounting a campaign for stronger regulatory authority by publicizing a list of injurious products that had been ruled permissible under the 1906 law, including radioactive beverages, mascara that could cause blindness, and worthless "cures" for diabetes and tuberculosis. The resulting proposed law did not get through the Congress of the United States for five years, but was rapidly enacted into law following the public outcry over the 1937 Elixir Sulfanilamide tragedy, in which over 100 people died after using a drug formulated with a toxic, untested solvent.{{cite journal | vauthors = Hamowy R |title=Medical Disasters and the Growth of FDA |date=February 2010 |page=7 |journal=Independent Policy Reports |url=http://www.independent.org/pdf/policy_reports/2010-02-10-fda.pdf |access-date=January 14, 2022 |archive-date=October 10, 2011 |archive-url=https://web.archive.org/web/20111010101720/http://independent.org/pdf/policy_reports/2010-02-10-fda.pdf |url-status=live}}

President Franklin Delano Roosevelt signed the Federal Food, Drug, and Cosmetic Act into law on June 24, 1938. The new law significantly increased federal regulatory authority over drugs by mandating a pre-market review of the safety of all new drugs, as well as banning false therapeutic claims in drug labeling without requiring that the FDA prove fraudulent intent. The law also authorized the FDA to issue minimum food standards of identity for all mass-produced foods to reduce food fraud.{{Cite journal | vauthors = Frohlich X |date=March 2022 |title=Making Food Standard: The U.S. Food and Drug Administration's Food Standards of Identity, 1930s–1960s |url=https://www.cambridge.org/core/journals/business-history-review/article/abs/making-food-standard-the-us-food-and-drug-administrations-food-standards-of-identity-1930s1960s/367324CEA5135BFCD1CF1B0E24496F78 |journal=Business History Review |language=en |volume=96 |issue=1 |pages=145–176 |doi=10.1017/S0007680521000726 |issn=0007-6805|url-access=subscription }}

Soon after passage of the 1938 Act, the FDA began to designate certain drugs as safe for use only under the supervision of a medical professional, and the category of "prescription-only" drugs was securely codified into law by the Durham-Humphrey Amendment in 1951. These developments confirmed extensive powers for the FDA to enforce post-marketing recalls of ineffective drugs.

File:Examining New Drug Applications (067) (7184535293).jpg

Outside of the US, the drug thalidomide was marketed for the relief of general nausea and morning sickness, but caused birth defects and even the death of thousands of babies when taken during pregnancy.{{cite web | url = http://www.library.arizona.edu/exhibits/udall/congrept/87th/620817.html | title = Report of Congressman Morris Udall on thalidomide and the Kefauver hearings | publisher = University of Arizona Library | archive-url = https://web.archive.org/web/20100729124333/http://www.library.arizona.edu/exhibits/udall/congrept/87th/620817.html | archive-date=July 29, 2010 }} American mothers were largely unaffected as Frances Oldham Kelsey of the FDA refused to authorize the medication for market. In 1962, the Kefauver-Harris Amendment to the FD&C Act was passed, which represented a "revolution" in FDA regulatory authority.{{cite journal | vauthors = Temple R | title = Policy developments in regulatory approval | journal = Statistics in Medicine | volume = 21 | issue = 19 | pages = 2939–2948 | date = October 2002 | pmid = 12325110 | doi = 10.1002/sim.1298 | url = https://zenodo.org/record/1229361 | access-date = June 19, 2019 | url-status = live | s2cid = 24779317 | archive-url = https://web.archive.org/web/20181127125144/https://zenodo.org/record/1229361 | archive-date = November 27, 2018 }} The most important change was the requirement that all new drug applications demonstrate "substantial evidence" of the drug's efficacy for a marketed indication, in addition to the existing requirement for pre-marketing demonstration of safety. This marked the start of the FDA approval process in its modern form.

These reforms had the effect of increasing the time, and the difficulty, required to bring a drug to market.{{Cite book |title=How We Got Here: The '70s | vauthors = Frum D |author-link=David Frum |year=2000 |publisher=Basic Books |location=New York, New York |isbn=978-0-465-04195-4 |page=[https://archive.org/details/howwegothere70sd00frum/page/180 180] |url=https://archive.org/details/howwegothere70sd00frum/page/180}} One of the most important statutes in establishing the modern American pharmaceutical market was the 1984 Drug Price Competition and Patent Term Restoration Act, more commonly known as the "Hatch-Waxman Act" after its chief sponsors. The act extended the patent exclusivity terms of new drugs, and tied those extensions, in part, to the length of the FDA approval process for each individual drug. For generic manufacturers, the Act created a new approval mechanism, the Abbreviated New Drug Application (ANDA), in which the generic drug manufacturer need only demonstrate that their generic formulation has the same active ingredient, route of administration, dosage form, strength, and pharmacokinetic properties ("bioequivalence") as the corresponding brand-name drug. This Act has been credited with, in essence, creating the modern generic drug industry.{{cite journal | vauthors = Karki L |year=2005 |title=Review of FDA Law Related to Pharmaceuticals: The Hatch-Waxman Act, Regulatory Amendments and Implications for Drug Patent Enforcement |journal=Journal of the Patent & Trademark Office Society |volume=87 |pages=602–620}}

Concerns about the length of the drug approval process were brought to the fore early in the AIDS epidemic. In the mid- and late 1980s, ACT-UP and other HIV activist organizations accused the FDA of unnecessarily delaying the approval of medications to fight HIV and opportunistic infections.{{cite web |url=http://www.actupny.org/documents/cron-88.html |title=ACT UP/NY Chronology 1988 |access-date=March 14, 2015 |archive-date=February 2, 1998 |archive-url=https://web.archive.org/web/19980202195639/http://www.actupny.org/documents/cron-88.html |url-status=live}} Partly in response to these criticisms, the FDA issued new rules to expedite approval of drugs for life-threatening diseases, and expanded pre-approval access to drugs for patients with limited treatment options.{{cite web |url=https://www.fda.gov/ForConsumers/ByAudience/ForPatientAdvocates/SpeedingAccesstoImportantNewTherapies/ucm181838.htm |title=FDA Website: Expanded Access and Expedited Approval of New Therapies Related to HIV/AIDS |website=Food and Drug Administration |archive-date=November 1, 2013 |archive-url=https://web.archive.org/web/20131101115339/https://www.fda.gov/ForConsumers/ByAudience/ForPatientAdvocates/SpeedingAccesstoImportantNewTherapies/ucm181838.htm}} All of the initial drugs approved for the treatment of HIV/AIDS were approved through these accelerated approval mechanisms.{{cite web |url=https://www.fda.gov/fdac/special/newdrug/speeding.html |title=FDA report on accelerated approval process |website=Food and Drug Administration |archive-date=May 25, 2009 |archive-url=https://web.archive.org/web/20090525082655/https://www.fda.gov/fdac/special/newdrug/speeding.html}} Frank Young, then commissioner of the FDA, was behind the Action Plan Phase II, established in August 1987 for quicker approval of AIDS medication.{{Cite journal |title=Reagan, Regulation, and the FDA: The US Food and Drug Administration's Response to HIV/AIDS, 1980–90 | vauthors = Richert L |date=2009 |journal=Canadian Journal of History |volume=44 |issue=3 |pages=467–488 |doi=10.3138/cjh.44.3.467}}

In two instances, state governments have sought to legalize drugs that the FDA has not approved. Under the theory that federal law, passed pursuant to Constitutional authority, overrules conflicting state laws, federal authorities still claim the authority to seize, arrest, and prosecute for possession and sales of these substances,{{citation needed|date=June 2014}} even in states where they are legal under state law. The first wave was the legalization by 27 states of laetrile in the late 1970s. This drug was used as a treatment for cancer, but scientific studies both before and after this legislative trend found it ineffective.{{cite web |url=https://www.npr.org/templates/transcript/transcript.php?storyId=127773447 |title=Medicinal Marijuana: A Patient-Driven Phenomenon |date=June 14, 2010 |work=NPR.org |access-date=March 14, 2015 |archive-date=March 17, 2015 |archive-url=https://web.archive.org/web/20150317084419/http://www.npr.org/templates/transcript/transcript.php?storyId=127773447 |url-status=live}}{{cite web |url=http://www.quackwatch.com/01QuackeryRelatedTopics/Cancer/laetrile.html |title=The Rise and Fall of Laetrile |access-date=March 14, 2015 |archive-date=July 19, 2018 |archive-url=https://web.archive.org/web/20180719022002/http://www.quackwatch.com/01QuackeryRelatedTopics/Cancer/laetrile.html |url-status=live}} The second wave concerned medical marijuana in the 1990s and 2000s. Though Virginia passed legislation allowing doctors to recommend cannabis for glaucoma or the side effects of chemotherapy, a more widespread trend began in California with the Compassionate Use Act of 1996.

When the FDA requested Endo Pharmaceuticals on June 8, 2017, to remove oxymorphone hydrochloride from the market, it was the first request in FDA history to recall an effective drug over its potential for misuse.{{cite press release |date=June 8, 2017 |url=https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm562401.htm |title=FDA requests removal of Opana ER for risks related to abuse |publisher=Food and Drug Administration |access-date=October 26, 2017 |quote=Today, the U.S. Food and Drug Administration requested that Endo Pharmaceuticals remove its opioid pain medication, reformulated Opana ER (oxymorphone hydrochloride), from the market... This is the first time the agency has taken steps to remove a currently marketed opioid pain medication from sale due to the public health consequences of abuse...[FDA Commissioner Scott Gottlieb, M.D.]: "We are facing an opioid epidemic – a public health crisis, and we must take all necessary steps to reduce the scope of opioid misuse and abuse. |archive-date=November 4, 2017 |archive-url=https://web.archive.org/web/20171104114609/https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm562401.htm |url-status=dead}}

In February 2025, FDA food division head Jim Jones quit in protest of the "indiscriminate" layoffs of 89 staff members by the Donald Trump administration.{{cite news |last1=Gedeon |first1=Joseph |title=Food head at FDA quits citing Trump administration's mass staff cuts |url=https://www.theguardian.com/us-news/2025/feb/18/fda-food-head-quits-trump |access-date=February 18, 2025 |work=The Guardian |date=February 18, 2025}}

In May 2025, the FDA announced a ban on COVID-19 vaccine booster shots for all patients under the age of 65 or those with severe pre-existing conditions, saying that the data showing evidence of benefit for those under the age of 65 as “insufficient” and “at a high risk of bias”. Those under 65 who seek the vaccines anyway may be given a placebo to test the effects.{{Cite news |last=Jewett |first=Christina |last2=Mandavilli |first2=Apoorva |date=2025-05-20 |title=F.D.A. Poised to Restrict Access to Covid Vaccines |url=https://www.nytimes.com/2025/05/20/health/fda-covid-vaccines.html |access-date=2025-05-20 |work=The New York Times |language=en-US |issn=0362-4331}}

The Critical Path Initiative{{cite web |url=https://www.fda.gov/ScienceResearch/SpecialTopics/CriticalPathInitiative/default.htm |title=Critical Path Initiative | author = Office of the Commissioner |publisher=Food and Drug Administration |date=February 8, 2019 |access-date=December 16, 2019 |archive-date=April 22, 2019 |archive-url=https://web.archive.org/web/20190422171814/https://www.fda.gov/ScienceResearch/SpecialTopics/CriticalPathInitiative/default.htm |url-status=dead}} is the FDA's effort to stimulate and facilitate a national effort to modernize the sciences through which FDA-regulated products are developed, evaluated, and manufactured. The Initiative was launched in March 2004, with the release of a report entitled Innovation/Stagnation: Challenge and Opportunity on the Critical Path to New Medical Products.{{cite web | url = https://www.fda.gov/ScienceResearch/SpecialTopics/CriticalPathInitiative/CriticalPathOpportunitiesReports/ucm077262.htm | title = Innovation or Stagnation: Challenge and Opportunity on the Critical Path to New Medical Products | archive-url = https://wayback.archive-it.org/7993/20180125032208/https://www.fda.gov/ScienceResearch/SpecialTopics/CriticalPathInitiative/CriticalPathOpportunitiesReports/ucm077262.htm | archive-date=January 25, 2018 | publisher = U.S. Food and Drug Administration | access-date = August 30, 2012 }}

The Compassionate Investigational New Drug program was created after Randall v. U.S. ruled in favor of Robert C. Randall in 1978, creating a program for medical marijuana.{{cite web |url=https://www.vice.com/en/article/the-us-government-has-sent-this-guy-300-joints-each-month-for-34-years/ |title=The US Government Has Sent This Guy 300 Joints Each Month for 34 Years |date=September 9, 2016 |access-date=October 14, 2017 |archive-date=October 14, 2017 |archive-url=https://web.archive.org/web/20171014142910/https://www.vice.com/en_us/article/dp3e4y/the-us-government-has-sent-this-guy-300-joints-each-month-for-34-years |url-status=live}}

A 2006 court case, Abigail Alliance v. von Eschenbach, would have forced radical changes in FDA regulation of unapproved drugs. The Abigail Alliance argued that the FDA must license drugs for use by terminally ill patients with "desperate diagnoses", after they have completed Phase I testing.{{cite web |url=http://www.abigail-alliance.org/WLF_FDA.pdf |title=Abigail Alliance Citizen Petition to FDA |access-date=March 11, 2007 |archive-url=https://web.archive.org/web/20070221153207/http://abigail-alliance.org/WLF_FDA.pdf |archive-date=February 21, 2007}} {{small|(119 KB)}} The case won an initial appeal in May 2006, but that decision was reversed by a March 2007 rehearing. The US Supreme Court declined to hear the case, and the final decision denied the existence of a right to unapproved medications.

Critics of the FDA's regulatory power argue that the FDA takes too long to approve drugs that might ease pain and human suffering faster if brought to market sooner. The AIDS crisis created some political efforts to streamline the approval process. However, these limited reforms were targeted for AIDS drugs, not for the broader market. This has led to the call for more robust and enduring reforms that would allow patients, under the care of their doctors, access to drugs that have passed the first round of clinical trials.{{cite book | vauthors = Madden BJ |url=https://archive.org/details/freetochoosemedi0000madd |title=Free To Choose Medicine: How Faster Access to New Drugs Would Save Countless Lives and End Needless Suffering: Bartley J. Madden: 9781934791325: Amazon.com: Books |date=July 2010 |publisher=Heartland Institute |isbn=978-1-934791-32-5}}{{cite news |url=https://www.wsj.com/articles/SB10001424052702303812104576441610360466984 |work=The Wall Street Journal | vauthors = Boldrin M, Swamidass SJ |title=A New Bargain for Drug Approvals |date=July 25, 2011 |url-access=subscription |access-date=August 3, 2017 |archive-date=July 9, 2017 |archive-url=https://web.archive.org/web/20170709173632/https://www.wsj.com/articles/SB10001424052702303812104576441610360466984 |url-status=live}}

The widely publicized recall of Vioxx, a non-steroidal anti-inflammatory drug (NSAID) now estimated to have contributed to fatal heart attacks in thousands of Americans, played a strong role in driving a new wave of safety reforms at both the FDA rulemaking and statutory levels. The FDA approved Vioxx in 1999, and initially hoped it would be safer than previous NSAIDs due to its reduced risk of intestinal tract bleeding. However, a number of pre and post-marketing studies suggested that Vioxx might increase the risk of myocardial infarction, and results from the APPROVe trial in 2004 conclusively demonstrated this.{{cite journal | vauthors = Bresalier RS, Sandler RS, Quan H, Bolognese JA, Oxenius B, Horgan K, Lines C, Riddell R, Morton D, Lanas A, Konstam MA, Baron JA | title = Cardiovascular events associated with rofecoxib in a colorectal adenoma chemoprevention trial | journal = The New England Journal of Medicine | volume = 352 | issue = 11 | pages = 1092–1102 | date = March 2005 | pmid = 15713943 | doi = 10.1056/NEJMoa050493 | s2cid = 8161299 | doi-access = free }}

Faced with numerous lawsuits, the manufacturer voluntarily withdrew it from the market. The example of Vioxx has been prominent in an ongoing debate over whether new drugs should be evaluated on the basis of their absolute safety, or their safety relative to existing treatments for a given condition. In the wake of the Vioxx recall, there were widespread calls by major newspapers, medical journals, consumer advocacy organizations, lawmakers, and FDA officials{{cite web |url=http://www.finance.senate.gov/imo/media/doc/111804dgtest.pdf |title=David Graham's 2004 testimony to Congress |access-date=August 30, 2012 |archive-date=September 25, 2012 |archive-url=https://web.archive.org/web/20120925094651/http://www.finance.senate.gov/imo/media/doc/111804dgtest.pdf |url-status=live}} {{small|(28.3 KB)}} Retrieved August 30, 2012. for reforms in the FDA's procedures for pre- and post-market drug safety regulation.

In 2006, a Congressional committee was appointed by the Institute of Medicine to review pharmaceutical safety regulation in the U.S. and to issue recommendations for improvements. The committee was composed of 16 experts, including leaders in clinical medicine medical research, economics, biostatistics, law, public policy, public health, and the allied health professions, as well as current and former executives from the pharmaceutical, hospital, and health insurance industries. The authors found major deficiencies in the current FDA system for ensuring the safety of drugs on the American market. Overall, the authors called for an increase in the regulatory powers, funding, and independence of the FDA.{{Cite web | vauthors = Henderson D |title=Panel: FDA needs more power, funds |work=The Boston Globe |date=September 23, 2006 | url = http://www.boston.com/business/healthcare/articles/2006/09/23/panel_fda_needs_more_power_funds/ | archive-url = https://web.archive.org/web/20121023223500/http://www.boston.com/business/healthcare/articles/2006/09/23/panel_fda_needs_more_power_funds/ | archive-date = October 23, 2012 }}{{cite book | chapter-url = http://www.nap.edu/openbook.php?record_id=11750&page=205 | publisher = Books.nap.edu | archive-url = https://web.archive.org/web/20121025132523/http://www.nap.edu/openbook.php?record_id=11750&page=205 | archive-date=October 25, 2012 | chapter = Executive Summary of the 2006 IOM Report | title = The Future of Drug Safety: Promoting and Protecting the Health of the Public | date = 2007 | doi = 10.17226/11750 | isbn = 978-0-309-10304-6 }} Some of the committee's recommendations were incorporated into drafts of the PDUFA IV amendment, which was signed into law as the Food and Drug Administration Amendments Act of 2007.{{cite web |url=https://www.fda.gov/oc/initiatives/advance/fdaaa.html |title=Food and Drug Administration Amendments Act (FDAAA) of 2007 |publisher=Food and Drug Administration |access-date=March 14, 2015 |archive-date=May 25, 2009 |archive-url=https://web.archive.org/web/20090525082137/http://www.fda.gov/oc/initiatives/advance/fdaaa.html |url-status=dead}}

As of 2011, Risk Minimization Action Plans (RiskMAPS) have been created to ensure risks of a drug never outweigh the benefits of that drug within the post-marketing period. This program requires that manufacturers design and implement periodic assessments of their programs' effectiveness. The Risk Minimization Action Plans are set in place depending on the overall level of risk a prescription drug is likely to pose to the public.{{cite journal | vauthors = Qato DM, Alexander GC | title = Improving the Food and Drug Administration's mandate to ensure postmarketing drug safety | journal = JAMA | volume = 306 | issue = 14 | pages = 1595–1596 | date = October 2011 | pmid = 21990303 | doi = 10.1001/jama.2011.1457 }}

Prior to the 1990s, only 20% of all drugs prescribed for children in the United States were tested for safety or efficacy in a pediatric population.{{cite journal | vauthors = Temeck J |title=Pediatric Product Development in the U.S. |journal=FDA Seminar, Copenhagen |date=November 2010}} This became a major concern of pediatricians as evidence accumulated that the physiological response of children to many drugs differed significantly from those drugs' effects on adults. Children react differently to the drugs because of many reasons, including size, weight, etc. There were several reasons that few medical trials were done with children. For many drugs, children represented such a small proportion of the potential market, that drug manufacturers did not see such testing as cost-effective.

Also, the belief that children are ethically restricted in their ability to give informed consent brought increased governmental and institutional hurdles to approval of these clinical trials, and greater concerns about legal liability. Thus, for decades, most medicines prescribed to children in the U.S. were done so in a non-FDA-approved, "off-label" manner, with dosages "extrapolated" from adult data through body weight and body-surface-area calculations.

In an initial FDA attempt to address this issue they produced the 1994 FDA Final Rule on Pediatric Labeling and Extrapolation, which allowed manufacturers to add pediatric labeling information, but required drugs that had not been tested for pediatric safety and efficacy to bear a disclaimer to that effect. However, this rule failed to motivate many drug companies to conduct additional pediatric drug trials. In 1997, the FDA proposed a rule to require pediatric drug trials from the sponsors of New Drug Applications. However, this new rule was successfully preempted in federal court as exceeding the FDA's statutory authority.{{Cite journal |author=Politis P |year=2005 |title=Transition From the Carrot to the Stick: The Evolution of Pharmaceutical Regulations Concerning Pediatric Drug Testing |journal=Widener Law Review |volume=12 |page=271}}

While this debate was unfolding, Congress used the Food and Drug Administration Modernization Act of 1997 to pass incentives that gave pharmaceutical manufacturers a six-month patent term extension on new drugs submitted with pediatric trial data. The Best Pharmaceuticals for Children Act of 2007 reauthorized these provisions and allowed the FDA to request NIH-sponsored testing for pediatric drug testing, although these requests are subject to NIH funding constraints. In the Pediatric Research Equity Act of 2003, Congress codified the FDA's authority to mandate manufacturer-sponsored pediatric drug trials for certain drugs as a "last resort" if incentives and publicly funded mechanisms proved inadequate.

The priority review voucher is a provision of the Food and Drug Administration Amendments Act of 2007, which awards a transferable "priority review voucher" to any company that obtains approval for a treatment for a neglected tropical diseases. The system was first proposed by Duke University faculty David Ridley, Henry Grabowski, and Jeffrey Moe in their 2006 Health Affairs paper: "Developing Drugs for Developing Countries".{{cite journal | vauthors = Ridley DB, Grabowski HG, Moe JL | title = Developing drugs for developing countries | journal = Health Affairs | volume = 25 | issue = 2 | pages = 313–324 | year = 2006 | pmid = 16522573 | doi = 10.1377/hlthaff.25.2.313 | hdl-access = free | doi-access = free | hdl = 10161/7017 }} President Obama signed into law the Food and Drug Administration Safety and Innovation Act of 2012, which extended the authorization until 2017.{{cite web |url=http://www.gpo.gov/fdsys/pkg/PLAW-112publ144/pdf/PLAW-112publ144.pdf |title=Section 529 Rare Pediatric Disease Priority Review Voucher Incentive Program, Public Law 112-144 |publisher=Public Law |date=July 9, 2012 |access-date=November 19, 2015 |archive-date=March 6, 2016 |archive-url=https://web.archive.org/web/20160306214504/https://www.gpo.gov/fdsys/pkg/PLAW-112publ144/pdf/PLAW-112publ144.pdf |url-status=live}}

Since the 1990s, many successful new drugs for the treatment of cancer, autoimmune diseases, and other conditions have been protein-based biotechnology drugs, regulated by the Center for Biologics Evaluation and Research. Many of these drugs are extremely expensive; for example, the anti-cancer drug Avastin costs $55,000 for a year of treatment,{{Cite web |title=The Avastin Paradox |url=https://www.technologyreview.com/2009/07/13/30529/the-avastin-paradox/ |access-date=January 6, 2022 |website=MIT Technology Review |language=en |archive-date=January 6, 2022 |archive-url=https://web.archive.org/web/20220106123457/https://www.technologyreview.com/2009/07/13/30529/the-avastin-paradox/ |url-status=live }} while the enzyme replacement therapy drug Cerezyme costs $200,000 per year, and must be taken by Gaucher's disease patients for life.{{cite web |url=https://www.govtrack.us/congress/bills/110/hr1038 |title=To amend the Public Health Service Act to provide for the licensing of comparable and interchangeable biological products, and for other purposes. (2007; 110th Congress H.R. 1038) – GovTrack.us |work=GovTrack.us |access-date=March 14, 2015 |archive-date=January 12, 2015 |archive-url=https://web.archive.org/web/20150112032213/https://www.govtrack.us/congress/bills/110/hr1038 |url-status=live}}

Biotechnology drugs do not have the simple, readily verifiable chemical structures of conventional drugs, and are produced through complex, often proprietary, techniques, such as transgenic mammalian cell cultures. Because of these complexities, the 1984 Hatch-Waxman Act did not include biologics in the Abbreviated New Drug Application (ANDA) process. This precluded the possibility of generic drug competition for biotechnology drugs. In February 2007, identical bills were introduced into the House to create an ANDA process for the approval of generic biologics, but were not passed.

In 2013, a guidance was issued to regulate mobile medical applications and protect users from their unintended use. This guidance distinguishes the apps subjected to regulation based on the marketing claims of the apps.{{cite web |url=https://www.fda.gov/MedicalDevices/ProductsandMedicalProcedures/ConnectedHealth/MobileMedicalApplications/ucm255978.htm |title=Mobile Medical Applications |publisher=Food and Drug Administration |access-date=March 14, 2015 |archive-date=September 4, 2015 |archive-url=https://web.archive.org/web/20150904095950/http://www.fda.gov/MedicalDevices/ProductsandMedicalProcedures/ConnectedHealth/MobileMedicalApplications/ucm255978.htm |url-status=dead}} Incorporation of the guidelines during the development phase of these apps has been proposed for expedited market entry and clearance.{{cite journal | vauthors = Yetisen AK, Martinez-Hurtado JL, da Cruz Vasconcellos F, Simsekler MC, Akram MS, Lowe CR | title = The regulation of mobile medical applications | journal = Lab on a Chip | volume = 14 | issue = 5 | pages = 833–840 | date = March 2014 | pmid = 24425070 | doi = 10.1039/C3LC51235E }}

To standardize, automate and streamline the flow of regulatory data, FDA introduced an Electronic Submissions Gateway (ESG) in 2006. This gateway allows reporting organizations to send regulatory submissions to different centers over the internet, packaged in a center-specific format and enveloped as a GNU-compatible .tar.gz file, through either a FDA-specific WebTrader application{{cite web |title=Setting up a WebTrader Account Checklist |url=https://www.fda.gov/industry/create-esg-account/setting-webtrader-account-checklist | publisher = U.S. Food and Drug Administ ration|date=May 12, 2023 }}{{dead link|date=May 2025|bot=medic}}{{cbignore|bot=medic}} or via a more generic B2B communication protocol called AS2 (Applicability Statement 2).{{cite web |title=AS2 Protocol |url=https://aayutechnologies.com/docs/as2/as2-protocol/ |website=Aayu Technologies}}

For WebTrader, which is recommended for manual, small-volume submissions, users would typically install a client application{{cite web |title=Food and Drug Administration |url=https://www.fda.gov/media/156910/download?attachment | publisher = U.S. Food and Drug Administ ration}} on their computers and upload the package through it to FDA server. In AS2, which is recommended for automated or high-volume submissions, users can use any standard AS2 software to transmit the package to FDA by including additional routing details on top of standard AS2, in the form of custom HTTP request headers.{{cite web |title=ESG Appendix F: AS2 Header Attributes |url=https://www.fda.gov/industry/about-esg/esg-appendix-f-as2-header-attributes | publisher = U.S. Food and Drug Administ ration|date=June 10, 2024 }}

{{Main|Criticism of the Food and Drug Administration}}

File:Comparison of pasta with sliced franks in tomato sauce with dried white beans based on the FDA Nutrition Facts label and the proposed Nutrition Facts label.pdf

The FDA has regulatory oversight over a large array of products that affect the health and life of American citizens. As a result, the FDA's powers and decisions are carefully monitored by several governmental and non-governmental organizations. A $1.8{{nbsp}}million 2006 Institute of Medicine report on pharmaceutical regulation in the U.S. found major deficiencies in the current FDA system for ensuring the safety of drugs on the American market. Overall, the authors called for an increase in the regulatory powers, funding, and independence of the FDA.{{Cite web |date=July 2, 2010 |title=The Future of Drug Safety: Promoting and Protecting the Health of the Public |url=http://www.nap.edu/catalog.php?record_id=11750 |archive-url=https://web.archive.org/web/20100702001617/http://www.nap.edu/catalog.php?record_id=11750 |archive-date=July 2, 2010 |access-date=January 2, 2025 |website=nap.edu}}

A 2022 article from Politico raised concerns that food is not a high priority at the FDA. The report explains the FDA has structural and leadership problems in the food division and is often deferential to industry.{{cite web | vauthors = Bottemiller Evich H |title=How the FDA's food division fails to regulate health and safety hazards |url=https://www.politico.com/interactives/2022/fda-fails-regulate-food-health-safety-hazards/ |website=politico.com |publisher=Politico |access-date=April 4, 2022 |archive-date=April 9, 2022 |archive-url=https://web.archive.org/web/20220409111829/https://www.politico.com/interactives/2022/fda-fails-regulate-food-health-safety-hazards/ |url-status=live }} This might be attributed to lobbying and influence of big food companies in Washington, D.C.{{cite web | vauthors = Doering C |title=Where the dollars go: Lobbying a big business for large food and beverage CPGs |url=https://www.fooddive.com/news/where-the-dollars-go-lobbying-a-big-business-for-large-food-and-beverage-c/607982/ |website=fooddive.com |publisher=Food Dive |access-date=April 18, 2022 |archive-date=March 19, 2022 |archive-url=https://web.archive.org/web/20220319090710/https://www.fooddive.com/news/where-the-dollars-go-lobbying-a-big-business-for-large-food-and-beverage-c/607982/ |url-status=live }}

{{Portal bar|Food|United States|Law|Medicine}}

• Adverse reaction
• Adverse event
• Adverse drug reaction
• Biosecurity
• Biosecurity in the United States
• Drug Efficacy Study Implementation
• Food and Drug Administration Modernization Act of 1997
• FDA Food Safety Modernization Act of 2011
• FDA Fast Track Development Program (for drugs)
• Food and Drug Administration Amendments Act of 2007 (e.g. drugs)
• Food and Drug Administration Safety and Innovation Act of 2012 (GAIN/QIDP etc.)
• Inverse benefit law
• Investigational Device Exemption (for use in clinical trials)
• Kefauver Harris Amendment 1962 – required "proof-of-efficacy" for drugs

International:

• Food Administration
• International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH)
• African Union: African Medicines Agency
• Australia: Therapeutic Goods Administration
• Brazil: National Health Surveillance Agency
• Canada: Marketed Health Products Directorate
• Canada: Health Canada
• Denmark: Danish Medicines Agency
• European Union: European Medicines Agency
• Germany: Federal Institute for Drugs and Medical Devices
• India: Food Safety and Standards Authority of India
• India: Central Drugs Standard Control Organization
• Japan: Ministry of Health, Labour and Welfare (MHLW)
• Japan: Pharmaceuticals and Medical Devices Agency
• Mexico: Federal Commission for the Protection against Sanitary Risk
• Philippines: Food and Drug Administration (FDA)
• Singapore: Health Sciences Authority
• United Kingdom: Medicines and Healthcare products Regulatory Agency
• United States: Food and Drug Administration

{{NoteFoot}}

{{Reflist}}

{{refbegin|30em}}

• {{cite journal | vauthors = Givel M | title = Philip Morris' FDA gambit: good for public health? | journal = Journal of Public Health Policy | volume = 26 | issue = 4 | pages = 450–468 | date = December 2005 | pmid = 16392744 | doi = 10.1057/palgrave.jphp.3200032 }}
• {{cite encyclopedia | vauthors = Henninger D |author-link=Daniel Henninger |editor=David R. Henderson |encyclopedia=Concise Encyclopedia of Economics |title=Drug Lag |url=http://www.econlib.org/library/Enc1/DrugLag.html |year=2002 |edition=1st |publisher=Library of Economics and Liberty}} {{OCLC|317650570|50016270|163149563}}
• {{cite book | vauthors = Hilts PJ |title=Protecting America's Health: The FDA, Business, and One Hundred Years of Regulation |date=2003 |publisher=Alfred A. Knopf |location=New York |isbn=0-375-40466-X}}
• {{cite journal | vauthors = Fain K, Daubresse M, Alexander GC | title = The Food and Drug Administration Amendments Act and postmarketing commitments | journal = JAMA | volume = 310 | issue = 2 | pages = 202–4 | date = July 2013 | pmid = 23839755 | doi = 10.1001/jama.2013.7900 }}
• {{cite book | vauthors = Madden BJ | date = 2010 | title = Free To Choose Medicine: How Faster Access to New Drugs Would Save Countless Lives and End Needless Suffering | location = Chicago | publisher = The Heartland Institute | isbn = 978-1-934791-32-5 }}
• {{cite book |last1=Moore TJ |title=Prescription for Disaster: The Hidden Dangers in Your Medicine Cabinet |date=1998 |publisher=Simon & Schuster |location=New York, NY |isbn=0-684-82998-3}}
• {{cite book | vauthors = Obenchain J, Spark A |title=Food policy: looking forward from the past |date=2016 |publisher=CRC Press, Taylor & Francis Group |location=Boca Raton, FL |isbn=978-1-4398-8025-8}}
• {{cite journal | vauthors = Shah S, El-Sayed A |title=Medical Algorithms Need Better Regulation |journal=Scientific American |date=January 2022 |volume=326 |issue=1 |pages=10 |doi=10.1038/scientificamerican0122-10 |pmid=39016568 | quote = Medical algorithms are less transparent, far more complex, more likely to reflect preexisting human bias, and more apt to evolve (and fail) over time than medical devices in the past. }}

{{refend}}

{{Commons category}}

{{Wikinews category}}

• {{Official website}}
• [https://www.federalregister.gov/agencies/food-and-drug-administration Food and Drug Administration] in the Federal Register
• [https://www.ecfr.gov/current/title-21/chapter-I Food and Drug Administration] in the Code of Federal Regulations
• [https://web.archive.org/web/20130225130615/http://xml.fido.gov/stratml/carmel/FDAwStyle.xml Strategic Plan] (archived)
• {{OL author}}
• [https://onlinebooks.library.upenn.edu/webbin/book/lookupname?key=United+States.+Food+and+Drug+Administration Online books by United States Food and Drug Administration] at The Online Books Page
• [https://openomb.org/agency/department-of-health-and-human-services/bureau/food-and-drug-administration Food and Drug Administration] apportionments on OpenOMB

{{Food and Drug Administration}}

{{HHS agencies}}

{{Pharmaceutical industry in the United States}}

{{Consumer Food Safety}}

{{Authority control}}

{{DEFAULTSORT:Food And Drug Administration (United States)}}

Category:1906 establishments in the United States

Category:American medical research

Category:Government agencies established in 1906

Category:Regulators of biotechnology products

Category:National agencies for drug regulation