RCRC Independent Review Board has been a trusted and leading provider of professional IRB services for 25 years. RCRC provides IRB review for all phases of research in a variety of therapeutic areas and study designs in the pharmaceutical, biotech and medical device industries, and for single-site, multi-site and mega trials. They also provide ethical review for behavioral and social sciences research including, data collection, repository, surveys, outcomes and registries. They offer multiple meetings weekly with a 24-48 hour turnaround time employing 21 CFR Part 11compliant innovative technologies. RCRC developed SafeSync Online Submissions with 256-bit public key encryption and GlobeSync Virtual Workspace, a WEB-based document management portal allowing 24/7 secure access to IRB study documents. Fully accredited by the Association for Accreditation of Human Research Protection Programs, Inc. (AAHRPP), they are a group of experienced IRB members and professionals certified as CCRP, CIP, or CQPA. As a partner on your clinical trial, they are committed to providing quality, flexible and responsive service to assist in the successful and timely completion of research studies.