Multi-Site Studies

IRBco has a vast experience in reviewing research studies involving up to several thousand investigators. We offer free training to site staff and investigators and help them generate consent forms, recruitment materials etc. as needed.

Our expert staff works closely with site-coordinators and conducts thorough pre-reviews to provide the review board with necessary information to assist in timely and comprehensive board reviews. At IRBco, we are proud to have Board members with a wide range of clinical expertise to provide the highest standard of ethical reviews for your studies.

Our clients are provided with a single point of contact for all communication and oversight related to the project. Our state-of-the-art electronic submission system provides 24/7 tracking and access to all study submission materials. It expedites the submission process and reduces errors, again ensuring timely and efficient review of research. We are proud of our integrated systems approach to ascertain transparent communication between IRBco team and the respective Investigators, Sites, CRO’s and Sponsors.

Please contact us to learn more about the IRBco difference and other benefits of using IRBco for Multi-center studies.


IRBco is awarded Full Accreditation by the Association for the Accreditation of Human Research Protection Programs Inc. (AAHRPP). Accreditation validates our comprehensive program which integrates ethical reviews, state-of-the-art technology and staff development to create an environment of responsible and ethical human subject protection. We provide our services at levels beyond client expectations and that exceed federal requirements for safeguarding participants. We believe that accreditation leads to an increased level of professional accountability.

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