Human Research Protection Program Policies

HRPP Policies

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302.0     Human Research Protections Program Policy

302.1     Investigators as Study Participants

2.0            Institutional Review Board

3.0            Institutional Review Board Review Process

4.0            IRB Documentation and Records

5.0            Obtaining Informed Consent from Research Subjects

6.0            Vulnerable Subjects in Research

7.0             Investigational Drugs and Devices in Research

8.0            Unanticipated Problems Involving Risks to Subjects or Others

9.0            Protocol Deviations

10.0         Complaints and Non-Compliance

11.0           Reporting to Regulatory Agencies and Institutional Officials

12.0          Investigator Responsibilities

13.0          Quality Improvement in the HRPP Program

14.0          Participant Outreach Activities

15.0          Research Funded by the Department of Defense

16.0          Research Conducted by the Department of Education

17.0           Community Participatory Research

18.0          Electronic Signatures and Electronic Records

19.0          Deception or Incomplete Disclosure in Research

20.0         Internet Based Research

21.0          Collaborative Research Policy

Pennington Biomedical Research Center Combined HRPP Policies