A history of biopharmaceutics in the Food and Drug Administration 1968-1993
- PMID: 19936940
- PMCID: PMC2811644
- DOI: 10.1208/s12248-009-9154-8
A history of biopharmaceutics in the Food and Drug Administration 1968-1993
Abstract
The history of biopharmaceutics is reviewed, beginning with its origin out of the Division of Clinical Research in The Bureau of Medicine. The reason for the creation of the Division of Biopharmaceutics, the certification of Food and Drug Administration authority over the functions it was to have, and the implementation of that authority are described. The determination of bioequivalence, the bioavailability decision rules, pharmacokinetics, and drug metabolism are explained. The reason for the development of the Scale-Up and Post Approval Regulations and how they were developed are also explained.
References
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- U.S. Department of Health and Human Services. A brief history of the center for drug evaluation and research. 2009. http://www.fda.gov/cder/about/history/Histext.htm. Accessed March 2009.
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- U.S. Department of Health and Human Services. A brief history of the center for drug evaluation and research. 2009. http://www.fda.gov/aboutFDA/whatwedo/history/thisweek/ucm117833.htm.
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- United States of America versus Pharmadyne Laboratories and Bernard Bedrick; United States District Court, District of New Jersey. 1980.
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