IRB Policies

Below you will find a list of the most current UHCMC IRB Policies. The UHCMC IRB reviews its policies for adherence to current FDA and Institutional regulations every 3 years to ensure compliance. This policy review process is conducted to ensure appropriate maintenance of our AAHRPP accreditation as part of UHCMC’s commitment to the highest Human Research Protection standards. The FDA regulations pertinent to IRB’s include 21 CFR 50, Part 56, Part 312, and Part 812.

Administrative Policies

Types of New Research Studies

Maintenance of IRB Approved Research Studies

Vulnerable Subject Populations

Other Protocol Resources

Compliance in Research