美国FDA 指导原则 保护人类受试者可由IRB通过快速审查程序审查的研究类别 英文原版.pdfVIP

  • 24
  • 0
  • 约3.73万字
  • 约 4页
  • 2023-05-20 发布于四川
  • 举报

美国FDA 指导原则 保护人类受试者可由IRB通过快速审查程序审查的研究类别 英文原版.pdf

Federal Register / Vol. 63, No. 216 / Monday, November 9, 1998 / Notices 60353 DEPARTMENT OF HEALTH AND could be reviewed by the IRB through them at risk of criminal or civil liability HUMAN SERVICES the expedited review procedures set or be damaging to the subjects’ financial forth in the FDA’s regulations. OPRR standing, employability, insurability, Food and Drug Administration has a separate codification th

您可能关注的文档

文档评论(0)

1亿VIP精品文档

相关文档