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Statement of Practice: Remote Study Procedures
Secondary Use Research
Retention of Research Data/Biospecimens
Non-Significant Risk (NSR) Medical Devices: Monitoring Requirements
Updating IRB applications When Researcher(s) Leave U-M
Quality Assurance and Quality Improvement (QA/QI) Projects
Statement of Practice: HIPAA and U-M study team members outside Michigan Medicine in eResearch applications
Waivers and Alterations under OHRP, FDA and HIPAA
Protocol Resources
Multi-Site and Performance Site applications: Reporting to IRBMED
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.

Retention of Research Data/Biospecimens

Updated on:

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

Protocol Resources

Updated on: