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Start Over Subjects Ethics, Research ✖Remove constraint Subjects: Ethics, Research

2. 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.

3. Managing conflict of interest in AHCs to assure healthy industrial and societal relationships

Author(s):
Blue Ridge Academic Health Group, author.
Publication:
Atlanta, GA : Woodruff Health Sciences Center, Emory University, [2006]
Subject(s):
Academic Medical Centers -- ethics
Academic Medical Centers -- organization & administration
Conflict of Interest
Disclosure
Ethics, Professional
Ethics, Research
Public Policy
Humans
United States