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.
200 Series
IRB Authorities and Requirements
There are Currently No Attachments
300 Series
Investigator Responsibilities
There are Currently No Attachments
400 SeriesRegulatory Protections for Vulnerable Populations
There are Currently No Attachments
500 SeriesFDA Requirements for Human Subjects Research
There are Currently No Attachments
600 SeriesDoD Requirements for Human Subjects Research
There are Currently No Attachments
700 SeriesInternational Research Requirements
There are Currently No Attachments
800 SeriesCompliance and Research Event Reporting Requirements
There are Currently No Attachments
Active HRPP Policies (SOPs)
There are Currently No Attachments
Guidance
Regulations and Ethical Guidance
- 45 CFR 46 - The Common Rule
- The Belmont Report
- Search for Federalwide Assurances
- HHS Regulations and Policies Guidance
Overview
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