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FDA is issuing more postmarketing requirements, but challenges with oversight persist.

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Record details

  • Physical Description: 1 online resource (26 pages) : illustrations
  • Publisher: [Washington, D.C.] : Department of Health and Human Services, Office of Inspector General, 2016.

Content descriptions

General Note: Title from title screen (viewed Aug 9, 2016).
"July 2016."
Bibliography, etc. Note: Includes bibliographical references.
Subject: United States. Food and Drug Administration > Rules and practice.
Drugs > United States > Testing > Management.
Clinical trials > Government policy > United States.

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