Criticism of the Food and Drug Administration information
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Numerous governmental and non-governmental organizations have criticized the U. S. Food and Drug Administration for alleged excessive and/or insufficient regulation. The U.S. Food and Drug Administration (FDA) is an agency of the United States Department of Health and Human Services and is responsible for the safety regulation of most types of foods, dietary supplements, drugs, vaccines, biological medical products, blood products, medical devices, radiation-emitting devices, veterinary products, and cosmetics. The FDA also enforces section 361 of the Public Health Service Act and the associated regulations, including sanitation requirements on interstate travel as well as specific rules for control of disease on products ranging from animals sold as pets to donations of human blood and tissue.[1]
A $1.8 million 2006 Institute of Medicine report on pharmaceutical regulation in the U.S. found major deficiencies in the 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.[2][3][4]
^Swann, John P. (January 2, 2018). "FDA's Origin". Food and Drug Administration. Archived from the original on July 12, 2019. Retrieved July 12, 2019.
^Henderson, Diedtra (September 23, 2006). "Panel: FDA needs more power, funds". The Boston Globe. Archived from the original on October 23, 2012. Retrieved July 12, 2019.
^"The Future of Drug Safety: Action Steps for Congress (report brief)" (PDF). Institute of Medicine. September 2006. Archived from the original (PDF) on July 12, 2019. Retrieved July 12, 2019.
^Baciu, Alina; Stratton, Kathleen; Burke, Sheila P., eds. (2007). The Future of Drug Safety:Promoting and Protecting the Health of the Public. The National Academies Press. doi:10.17226/11750. ISBN 978-0-309-10304-6.
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