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Other Reportable Information or Occurrence (ORIO)
Research Involving Genetic, Genomic, and/or DNA Collection or Analysis
Secondary Use Research
Research Participants with Limited English Proficiency, Low Literacy, Vision Impairments, or Hearing Impairments
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

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.

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: