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
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
21.0 Collaborative Research Policy
Pennington Biomedical Research Center Combined HRPP Policies
