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1. 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.

2. Vetting peer reviewers at NIH’s Center for Scientific Review: strengths and limitations

Publication:: [Washington, D.C.] : U.S. Department of Health and Human Services, Office of Inspector General, September 2019
Subject(s):: Ethics, Research
Peer Group
Peer Review
Research
Scientific Misconduct
Confidentiality
Intellectual Property
Humans
United States
National Institutes of Health (U.S.)

3. NIH has made strides in reviewing financial conflicts of interest in extramural research, but could do more

Publication:: [Washington, D.C.] : U.S. Department of Health and Human Services, Office of Inspector General, September 2019
Subject(s):: Conflict of Interest
Ethics, Research
Research
Financing, Government
Government Regulation
Mandatory Programs
Humans
United States
National Institutes of Health (U.S.)

4. Human vivisection: a statement and an inquiry

Author(s):: American Humane Association.
Publication:: Chicago, Ill. : American Humane Association, 1899
Subject(s):: Vivisection
Human Experimentation
Ethics, Research