The United States Federal Drug Administration (FDA) and clinical research

Stephen P. Glasser, Carol M. Ashton, Nelda Wray

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

The USFDA is an agency of the US Department of Health and Human Services and is the nation's oldest consumer protection agency whose function it is to review drugs before marketing, monitor marketed drugs, monitor drug manufacturing and advertising, protect drug quality, and to conduct applied research. It is charged with overseeing of not only human drugs and biologics, but also veterinary drugs, foods, medical devices, and radiopharmaceuticals, and as such serves as a watch dog over industry. This chapter discusses the historical development of the FDA, and what the FDA is today. The phases of research development leading to the marketing of a new drug, the role of the FDA in surgical interventions, and the FDA's role in advertising and adverse event reporting are discussed.

Original languageEnglish (US)
Title of host publicationEssentials of Clinical Research
PublisherSpringer Netherlands
Pages93-110
Number of pages18
ISBN (Print)9781402084850
DOIs
StatePublished - Dec 1 2008

ASJC Scopus subject areas

  • Medicine(all)

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