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.
Izvorni zapis
Citati kopirani doslovno iz izvornog zapisa metode. Ne impliciraju nikakvu provjeru na razini tvrdnje.
- 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
Uređene tvrdnje
Tvrdnje pohranjene u knjigu dokaza, svaka s vlastitom procjenom.
Ovaj prikaz ne izmišlja procjenu tvrdnje kada knjiga dokaza nema nijednu.
Povezane metode
Generirano iz grafa metode i prikazano kao strojno predložene relacije — ne implicira se nikakva tvrdnja dokaza.