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Guidance
Suggested parameters and sets of instructions outlining best practices and standards for accomplishing specific duties.
Suggested parameters and sets of instructions outlining best practices and standards for accomplishing specific duties.
This Copy Was Generated On: April 24, 2025
Investigator Responsibilities
IRBMED
| Approval Date:
April 17, 2012 9:45 am
Department of Health and Human Services
Food and Drug Administration
Office of Human Research Protections
University of Michigan
- Human Research Protection Program, Operations Manual Part 6, Roles and Responsibilities of Investigators and Research Staff
- Required Reporting: Adverse Events, Other Reportable Information and Occurences, and Unanticipated Problems Involving Risks to Subjects and Others
Created 4/17/2012
Last reviewed (no revisions) October 30, 2023
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Edited By: [email protected]
Last Updated: December 13, 2024 10:45 AM