Types of Ethics Committees in Research
Research ethics committees are independent governance bodies established to review and oversee human subjects research. In the United States, these are called Institutional Review Boards (IRBs); in the United Kingdom and Commonwealth nations, Research Ethics Committees (RECs); and in European Union and other jurisdictions, they are termed Ethics Committees. These bodies operate under national regulations—45 CFR 46 in the U.S., the Medicines for Human Use (Clinical Trials) Regulations in the UK, and the EU Clinical Trials Regulation in Europe—to ensure research protects participant rights, safety, and welfare.
Source record
Citations copied verbatim from the method’s source record. No claim-level verification is inferred from them.
- U.S. Department of Health and Human Services. (2018). Protection of Human Subjects. Code of Federal Regulations Title 45, Part 46. · URL
- U.S. Food and Drug Administration. (2013). Institutional Review Boards: Frequently Asked Questions. Center for Drug Evaluation and Research. · URL
- International Council for Harmonisation. (2016). ICH Harmonised Guideline: Integrated Addendum to ICH E6(R1). Good Clinical Practice E6(R2). · URL
Curated claims
Claims persisted in the evidence ledger, each with its own assessment.
This view does not invent a claim assessment when the ledger has none.
Related methods
Generated from the method graph and shown as machine-suggested relations — no evidence claim is inferred.