IRB submission review

eagle-i ID

Resource Type

Properties

1. Resource Description

   IRB submission review (single and multi-center trials) Regulatory Knowledge and Support consultation may be able to shorten the time to approval with its experience and particular regulatory and ethics perspective. Clinical research coordinators and investigators can request a consult for BUCK-IRB submission training and associated concerns. This service is complementary to the assistance provided by the University’s Office of Responsible Research Practices (ORRP) and to the University’s overall Human Research Protection Program.

2. Service Provided by

   CCTS Regulatory Knowledge and Support

3. Part of Collection

   Center for Clinical and Translational Science (CCTS)

4. Part of Collection

   Office of Research Collection