Barbara D. Buch, M.D., Chair of the 907 Steering committee and the Associate Director for Medicine in FDA’s Center for Biologics Evaluation and Research, recently posted on FDA Voice her reflections on a focused action plan to support inclusion of diverse populations...
On November 18, 2010, Pearl IRB, a company providing clinical trial research institutional review board services and other key clinical trial assistance, received national certification as a Women’s Business Enterprise by the Great Lakes Women’s Business Enterprise...
Single IRB – A Guide to the Common Rule sIRB Mandate
The sIRB requirement is active. Is your study affected?
