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Reporting Time-Sensitive Modifications
Evaluating Risks to Participants
Single IRB (sIRB) and Cooperative Multi-Site Research
Retention of Research Data/Biospecimens
Non-Significant Risk (NSR) Medical Devices: Monitoring Requirements
Updating IRB applications When Researcher(s) Leave U-M
Emergency Research (Planned and Approved) with Exception from Informed Consent
Radiation Exposure Guide
Emergency Use of a Test Article in Life-Threatening Circumstances
Michigan Medicine Clinical Research Position Statement

Guidance

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

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:

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

Radiation Exposure Guide

Updated on: