Making clinical trials safer for human subjects

Am J Law Med. 2001;27(2-3):253-82.
No abstract available

MeSH terms

  • Adverse Drug Reaction Reporting Systems
  • Clinical Trials as Topic / standards*
  • Conflict of Interest
  • Disclosure
  • Ethics, Medical*
  • Federal Government
  • Genetic Therapy / adverse effects*
  • Government Regulation*
  • Human Experimentation*
  • Humans
  • National Institutes of Health (U.S.)
  • Research Support as Topic
  • Risk Management
  • Safety Management*
  • United States
  • United States Food and Drug Administration