Porovnať metódy

	Etická komisia pre výskum (Institutional Review Board – IRB)	Informovaný súhlas vo výskume
Odbor	Etika výskumu	Etika výskumu
Rodina	Process / pipeline	Process / pipeline
Rok vzniku	1974	1947
Tvorca	U.S. Federal Requirement (National Research Act 1974); International adoption by WMA and research institutions globally	Multiple (Nuremberg Code 1947 first principle; formalized in Belmont Report 1979, Declaration of Helsinki 1964; US Common Rule 45 CFR 46)
Typ	Standard	Guideline
Pôvodný zdroj	U.S. Code of Federal Regulations, Title 45, Part 46: Protection of Human Subjects. Office of the Federal Register.	U.S. Department of Health and Human Services. Code of Federal Regulations Title 45, Part 46: Protection of Human Subjects. Federal Register.
Ďalšie názvy	IRB, Research Ethics Committee, REC	Research Consent, Informed Consent Process
Príbuzné	4	4
Zhrnutie	The Institutional Review Board (IRB) is the independent ethics committee established at research institutions to review and approve human subjects research, ensuring compliance with ethical principles and federal regulations. Created as a legal requirement by the U.S. National Research Act (1974) and now adopted globally, the IRB serves as the primary mechanism for protecting research subjects while enabling legitimate research to proceed. No human subjects research can begin without IRB approval.	Informed consent is the cornerstone of ethical human subjects research, requiring researchers to disclose material information about a study and obtain voluntary agreement from subjects before participation. Established as the first principle of the Nuremberg Code (1947) and formalized in subsequent ethical frameworks (Declaration of Helsinki 1964, Belmont Report 1979), informed consent protects subject autonomy, enables risk-benefit assessment, and creates accountability. Effective informed consent requires far more than obtaining a signature—it demands clear communication, genuine comprehension, and authentic voluntariness.