This page contains password-protected links used by members of the boards in carrying out their reviews. For information about the IRBMED and a roster of the membership, visit the About IRBMED section.
Legacy Applications and Informed Consent Documents ('E-subs'); Other Work and Information Documents
- Secure Links
- Legacy Applications, Informed Consent and other supporting Documents. Help for the new xythos system can be found on the Xythos wiki.
- Resource Links
- UM Human Research Participants Protection Program Operations Manual
- IRBMED Guidelines for Determining When Assent Should be Required or Waived (PDF)
- HHS Office of Human Research Protections (OHRP)
- HHS Food and Drug Administration (FDA)