Subjects: Research Subjects / Genre: Technical Report - Digital Collections - National Library of Medicine Search Results

Start Over Subjects Research Subjects ✖ Genre Technical Report ✖ Publication Year 2017 ✖

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

Publication:: [Washington, D.C.] : U.S. Department of Health and Human Services, Office of Inspector General, July 2017
Subject(s):: Human Experimentation -- standards
Patient Rights
Research Subjects
Ethics Committees, Research
Guideline Adherence
Human Experimentation -- ethics
Humans
United States
United States. Department of Health and Human Services.
United States. Department of Health and Human Services. Office for Human Research Protections.

2. OHRP should inform potential complainants of how they can seek whistleblower protections:

Publication:: [Washington, D.C.] : U.S. Department of Health and Human Services, Office of Inspector General, September 2017
Subject(s):: Human Experimentation
Research Subjects
Whistleblowing
Disclosure
Humans
United States
United States. Department of Health and Human Services.

3. 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

Publication:: Silver Spring, MD : Center for Drug Evaluation and Research, July 2017
Subject(s):: Clinical Trials as Topic -- standards
Human Experimentation -- standards
Informed Consent -- standards
Ethics Committees, Research
Ethics, Research
Informed Consent -- ethics
Research Subjects
Risk
Humans
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.