Skip to main content
← U-M RESEARCH COMPLIANCE PROGRAMS
← Research A-Z Gateway
← Medical School Office of Research Homepage
Research A to Z
Menu
Templates
SOPs
Guidance
Policies
Informational
Glossary
About
Login
I'm Looking for Information About
Search
Browse by:
Content Type
Type
-Templates
-SOPs
-Guidance
-Policies
-Informational
Topic
Topic
Adverse Events & Other Reportable Information and Occurrences
Application Types
Billing
Clinical Research
Clinical Trial
eResearch Regulatory Management (eRRM)
FDA (Drugs, Devices & Biologics)
HIPAA & Protected Health Information
Indirect Cost
Informed Consent & Assent
International Research
Investigator & Study Team Responsibilities
OnCore
Post-Award
Pre-Award
Recruitment
Regulations & Policies (Federal, State & Local)
Repository
Single IRB (sIRB)
Statements of Practice
Subject Payments & Reimbursement
Subject Populations
Unit
Unit
Calendar Review & Analysis Office
Office of Graduate & Postdoctoral Studies
Institutional Review Boards (IRBMED)
Grant Services & Analysis
Data Office for Clinical & Translational Research
Clinical Trials Support Office
Central Biorepository
Apply
Investigator Initiated Protocol
Protocols that are written by a UM investigator.
© 2024
The Regents of the University of Michigan
--
U-M Gateway
Non-Discrimination Policy
--
Michigan Web Design by Boxcar Studio
