Trust Schulman
For over 25 years Schulman has been one of the leading independent IRBs in the country. We continue to find better ways for sponsors, CROs and sites to work easily with an IRB that provides the highest quality review services available.
Our secure WebPortal™ 3D and SiteAccess™ tools allow sponsors, CROs and sites to track their submissions to the IRB in real time and to easily download approval letters and other approved documents.
We have a superior audit history with FDA, having completed 4 (four) consecutive audits with no findings since 1987.
Our US and Canadian Boards are fully accredited by the Association for the Accreditation of Human Research Protection Programs (AAHRPP).
Turnaround times for the review of study protocols, investigative sites and study materials are very competitive without sacrificing quality and thoroughness.
Need more information about Schulman’s services and capabilities? Contact 
Business Development.