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1. OHRP generally conducted its compliance activities independently, but changes would strengthen its independence

3. E6(R2) good clinical practice: integrated addendum to ICH E6(R1)

5. 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 boards

6. Certificates of confidentiality: guidance for sponsors, sponsor-investigators, researchers, industry, and food and drug administration staff