IRB Services
Versiti Clinical Trial Services proudly offers AAHRPP-accredited IRB services for single-site, multi-site (single IRB/central IRB) and international review services for clinical trials. With support from dedicated client service managers, we streamline your review process with industry-leading turnaround times, expertise across the spectrum of therapeutic areas, comprehensive review services for phase I-IV research and more.
Our boards consist of qualified, knowledgeable experts; are appropriately comprised of both genders; and are racially and culturally diverse, satisfying the requirements of 21 CFR 56.107 and 45 CFR 46.107. Our boards include professionals with a variety of expertise spanning scientific, medical, legal and non-scientific industries. Additionally, our board members have industry experience in drug safety, drug development, regulatory and medical affairs, protocol development and monitoring, research science, patient/research participant advocacy, and working with vulnerable populations.