Multi-Site Studies
Welcome to Liberty IRB. This area is designed to meet the needs of Sponsors and CROs. Services are provided for Phase I- IV pharmaceutical, medical device, behavioral and biological studies. At Liberty IRB, we are dedicated in protecting all human research participants while providing you with exceptional service.
Our project management approach enables you to have one point of contact throughout the entire process.
Discounted IRB review rates are provided to sponsors who bring their multi-center studies in for review. The sponsor receives the financial incentive of paying less per site (after initial site) for full board review. This centralized review system allows faster site initiations, as well as, meeting sponsor budget considerations.
In preparation for submission, please follow the sponsor submission checklist. This document may also be found on our forms page.
A protocol may be submitted for IRB review prior to identifying the principal investigator sites. This allows for us to review the protocol and begin the process of developing the final informed consent form.
Secure electronic submission is available for sensitive documents through our secured client login.
Please contact us for a username and password.