Effective June 1, 2012
Table of Contents:
1 Human Research Protection Program (HRPP)
3 IRB Review Process
4 Documentation and Records
5 Obtaining Informed Consent from Research Participants
6 Vulnerable Participants in Research
7 Investigational Drugs & Devices in Research
8 Unanticipated Problems Involving Risks to Participants or Others
9 Complaints and Non-compliance
10 Reporting to Regulatory Agencies and Institutional Officials
11 Investigator Responsibilities
12 Special Topics
Update:
12/2011
PDF Attached:
