Policies
The NIH Human Research Protection Program (HRPP) Policies are under development. The implemented policies appear below under policy groupings organized by topic. Upon implementation the remaining policies will appear below in under the topic groupings. Until the policies are implemented, the HRPP Standard Operating Procedures (SOPs) remain in effect.
General and Structural Changes to the NIH HRPP Policies
100 Series
Institutional Authorities and Requirements
There are Currently No Attachments
200 Series
IRB Authorities and Requirements
There are Currently No Attachments
300 Series
Investigator Responsibilities
There are Currently No Attachments
800 Series
Compliance and Research Event Reporting Requirements
There are Currently No Attachments
Active HRPP Policies (SOPs)
There are Currently No Attachments
Guidance
Common Rule Bulletins
- Common Rule Bulletin #1: Key Information
- Common Rule Bulletin #2: Exemptions
- Common Rule Bulletin #3: Biospecimens/Data REquirements in ICF
- Common Rule Bulletin #4: Reasonable Person Standard in ICF
- Common Rule Bulletin #5: Posting of ICFs
- Common Rule Bulletin #6: Broad Consent
Human Subjects Research vs. Not Human Subjects Research (NHSR)
There are Currently No Attachments
Other Guidance Documents
There are Currently No Attachments
Overview
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