FDA attempting to overcome major roadblocks in monitoring drug safety

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*