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Humanitarian Use Device Requirements for U-M Physicians & Investigators
Other Reportable Information or Occurrence (ORIO)
Reporting Time-Sensitive Modifications
Establishment of Biospecimen Collections Within the Central Biorepository
Non-Significant Risk (NSR) Medical Devices: Monitoring Requirements
Updating IRB applications When Researcher(s) Leave U-M
Statement of Practice: IRBMED Communication Methods for Study Teams
Emergency Research (Planned and Approved) with Exception from Informed Consent
Emergency Use of a Test Article in Life-Threatening Circumstances
Statement of Practice: PEERRS Certification Requirements
G
Guidance
Suggested parameters and sets of instructions outlining best practices and standards for accomplishing specific duties.

Reporting Time-Sensitive Modifications

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