« Previous
Next »
Titles
- Certificates of confidentiality: guidance for sponsors, sponsor-investigators, researchers, industry, and food and drug administration staff1
- E6(R2) good clinical practice: integrated addendum to ICH E6(R1)1
- Human vivisection1
- IRB waiver or alteration of informed consent for clinical investigations involving no more than minimal risk to human subjects: guidance for sponsors, investigators, and institutional review boards1
- OHRP generally conducted its compliance activities independently, but changes would strengthen its independence1
- OHRP should inform potential complainants of how they can seek whistleblower protections: 1