FDA revises informed consent regulations for emergency research

IRB. 1995 Sep-Dec;17(5-6):19-22.
No abstract available

MeSH terms

  • Critical Illness
  • Emergency Medical Services*
  • Ethics Committees
  • Ethics Committees, Research
  • Federal Government
  • Government
  • Government Regulation*
  • Human Experimentation*
  • Humans
  • Informed Consent*
  • Research Subjects
  • Research*
  • Risk
  • Risk Assessment
  • Social Control, Formal*
  • Therapeutic Human Experimentation*
  • United States
  • United States Dept. of Health and Human Services
  • United States Food and Drug Administration*