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

This Copy Was Generated On: June 15, 2026

Protocol Resources

IRBMED

| Approval Date:

March 30, 2026 10:30 am

The information for this Guidance document is now hosted by the Human Research Protection Program (HRPP).

U-M HRPP Protocol Tools and Templates

The HRPP Protocol Templates are available both in .docx and (as a pilot project in 2025-6) through the Protocol Builder tool.

For assistance in protocol development, contact your departmental research administrator, MICHR Research Development Consultation, or Clinical Trials Support Office.

UNIT: Clinical Trials Support Office / Institutional Review Boards (IRBMED)

TOPICS: Clinical Research / Clinical Trial / Investigator & Study Team Responsibilities / Records / Regulations & Policies (Federal, State & Local)

TAGS: Protocol / Regulatory / Study Coordinator / Study Teams / U-M resource

Questions?

Contact us at [email protected] or 734-763-4768 / (Fax 734-763-1234)
2800 Plymouth Road, Ann Arbor, MI 48109-2800
A list of IRBMED staff is available at our website.

Edited By: [email protected]
Last Updated: March 30, 2026 10:30AM

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