Sidelining safety--the FDA's inadequate response to the IOM

N Engl J Med. 2007 Sep 6;357(10):960-3. doi: 10.1056/NEJMp078157.
No abstract available

MeSH terms

  • Drug Approval* / legislation & jurisprudence
  • Drug Approval* / methods
  • Drug-Related Side Effects and Adverse Reactions*
  • Government Regulation
  • Models, Organizational
  • National Academies of Science, Engineering, and Medicine, U.S., Health and Medicine Division*
  • Organizational Innovation
  • Product Surveillance, Postmarketing
  • United States
  • United States Food and Drug Administration / organization & administration*
  • United States Food and Drug Administration / standards