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.
Zdrojový záznam
Citácie skopírované doslovne zo zdrojového záznamu metódy. Nevyplýva z nich žiadne overenie na úrovni tvrdenia.
- 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
Spracované tvrdenia
Tvrdenia uložené v registri dôkazov, každé s vlastným hodnotením.
Tento pohľad nevymýšľa hodnotenie tvrdenia, ak register žiadne nemá.
Súvisiace metódy
Vygenerované z grafu metód a zobrazené ako vzťahy navrhnuté strojom – nevyplýva z nich žiadne tvrdenie o dôkaze.