Anonymous ID: 6a9fb4 Aug. 4, 2022, 3:47 p.m. No.17046289   🗄️.is 🔗kun   >>5270

>>17044646

 

The Bellmont Principals/policy are based on Nuremberg code

 

45 CFR 46

The HHS regulations for the protection of human subjects in research at 45CFR 46 include five subparts. Subpart A, also known as the Common Rule, provides a robust set of protections for research subjects; subparts B, C, and D provide additional protections for certain populations in research; and subpart E provides requirements for IRB registration. The Common Rule, subpart A, was revised in recent years. Access the regulatory language for all of the subparts using the links below. In addition, OHRP provides an annotated version of the Common Rule that highlights changes between the pre-2018 and 2018 versions of the Common Rule.

https://www.hhs.gov/ohrp/regulations-and-policy/regulations/45-cfr-46/index.html

 

Regulations

The U.S. Department of Health and Human Services codified it’s regulations for the protection of human subjects in research in the code of federal regulations at 45 C.F.R. 46, which includes five subparts. Below, readers can access the regulatory text of subpart A (the Common Rule), including the 2018 revisions to the Common Rule, and subparts B-E. OHRP also provides additional information about the revisions to the Common Rule, the preamble to the revised regulatory text, and the process of revising the Common Rule.

 

OHRP makes available the full text of the HHS regulations for the protection of human subjects in research (45 CFR 46), the Common Rule (45 CFR 46 Subpart A), and FDA human subject protection regulations.

45 CFR 46

 

Read the HHS Policy for Protection of Human Subjects at 45 CFR Part 46, including the two versions of the Common Rule at subpart A.

Revision of the Common Rule

 

Find more information about the revision of the Common Rule, including the preamble, timeline of the revisions, and list of related terminologies.

 

OHRP also makes available information about HHS’s statutory authority, the Federal Departments and Agencies that adhere to the Common Rule, and the U.S. Food and Drug Administration (FDA) regulations, including regulations for the protection of human subjects in research that falls under its jurisdiction

https://www.hhs.gov/ohrp/regulations-and-policy/regulations/regulatory-text/index.html#46.101