FDA attempting to overcome major roadblocks in monitoring drug safety

J Natl Cancer Inst. 2005 Jun 15;97(12):872-3. doi: 10.1093/jnci/97.12.872.
No abstract available

Publication types

  • News

MeSH terms

  • Adverse Drug Reaction Reporting Systems / legislation & jurisprudence
  • Adverse Drug Reaction Reporting Systems / standards
  • Clinical Trials Data Monitoring Committees
  • Drug Approval / legislation & jurisprudence*
  • Drug Industry / legislation & jurisprudence*
  • Drug-Related Side Effects and Adverse Reactions*
  • Humans
  • Legislation, Drug / trends
  • Product Surveillance, Postmarketing / methods*
  • Product Surveillance, Postmarketing / standards
  • United States
  • United States Food and Drug Administration*