In multiple-site studies of any phase, coordination between everyone is crucial to success. Quorum understands the importance of compliance, accuracy, reliability and expertise in the world of clinical research.
Our AAHRPP-accredited boards meet daily, so we review every type of submission every day of the week. We can issue approval documents as quickly as within a day of IRB approval; our feature-rich OnQ Portal allows for secure submissions and updates; and our dedicated staff is there to guide you and your investigators throughout the study.
Quorum offers an array of ancillary services that can improve your study’s performance. These special features can shorten timelines and improve communication:
- Early Engagement puts the right pieces in place before a protocol is submitted.
- Site Match and our site outreach help you find sites and get them started faster.
- Our translation services provide accurate and compliant study documents in any language.
- Electronic tools like the OnQ Portal and our site-specific teams support your researchers.
- Webinars, white papers, and other materials keep researchers informed.
Quorum has a knowledgeable roster of board members; robust, user-oriented processes; convenient electronic tools; and trained staff. We are ready to help you run a successful study, whether it involves one research site or thousands.
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