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Exempt Human Subjects Research
Humanitarian Use Device Requirements for U-M Physicians & Investigators
Other Reportable Information or Occurrence (ORIO)
Secondary Use Research
Reporting Time-Sensitive Modifications
Evaluating Risks to Participants
Retention of Research Data/Biospecimens
Non-Significant Risk (NSR) Medical Devices: Monitoring Requirements
Statement of Practice: IRBMED Communication Methods for Study Teams
Statement of Practice: PEERRS Certification Requirements
G
Guidance
Suggested parameters and sets of instructions outlining best practices and standards for accomplishing specific duties.

Exempt Human Subjects Research

Updated on:

G
Guidance
Suggested parameters and sets of instructions outlining best practices and standards for accomplishing specific duties.

Secondary Use Research

Updated on:

G
Guidance
Suggested parameters and sets of instructions outlining best practices and standards for accomplishing specific duties.

Reporting Time-Sensitive Modifications

Updated on:

G
Guidance
Suggested parameters and sets of instructions outlining best practices and standards for accomplishing specific duties.

Evaluating Risks to Participants

Updated on:

G
Guidance
Suggested parameters and sets of instructions outlining best practices and standards for accomplishing specific duties.

Retention of Research Data/Biospecimens

Updated on: