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The Association for the Accreditation of Human Research Protection Programs accredits high-quality human research protection programs to promote excellent, ethically sound research. AAHRPP accreditation means that Quorum has demonstrated a commitment to high standards of patient protection and regulatory compliance.
Quorum conducts a thorough quality check on all outgoing documents, to ensure that sites receive high quality approval documents that are free of errors.
We guarantee a 24-hour turnaround on eligible site submissions (from submission to document posting). And with a prompt amendment review cycle, plus expedited translation services, you’ll gain efficiencies when it matters most.
With easy-to-use online forms, multiple Board meetings a week, and a dedicated Site Support Team available from 5 AM PT – 5 PM PT, we deliver the fastest site start-up in the industry.
The OnQ™ portal is a powerful information hub providing sponsors, CROs and investigators immediate access to all Board correspondence, site start-up status as well as on-line submission capabilities.
Quorum’s submission paperwork focuses on collecting the information the IRB needs to know. Quorum’s submission paperwork focuses on collecting the information the IRB needs to know.
At Quorum, there’s no need to guess about who to call for assistance. Quorum assigns one Quorum representative to each study, and that person will serve as the single point of contact for the life of the study.
Quorum has one of the few ethics review boards accredited to review studies in both the United States and Canada*. Quorum can manage and coordinate submissions from either side of the 38th parallel using a single point of contact per study. * Certain provincial restrictions that apply to most other central REBs in Canada also apply to Quorum Review.
Quorum has worked with researchers from hundreds of institutions and we offer the same prompt turnaround times to our institutional researchers as we offer to our other researchers.
Our board has a deep knowledge and understanding of a broad range of therapeutic areas as well as medical devices, nutraceuticals, cosmetic products and social and behavioral research.
Quorum offers a dedicated Phase I team that is specially trained in the unique needs of Phase I studies. We offer flexibility and faster timelines in our Phase I processes.
With a streamlined submission process, aggressive volume pricing for large studies and rapid study start-up processes, we’re ideally prepared to support minimal risk research.