Central IRB (AARHPP-Accredited) with expedited reviews

BRANY’s central, AAHRPP-accredited IRB provides review for multi-center research projects. Our IRB is administered by experts in clinical research and human subject protection.

To learn more about the BRANY IRB, click here: http://www.branyirb.com/

  • Multidisciplinary expertise
    • Experts from leading academic centers serve as IRB members.
    • We combine the expertise of academics with the efficiency of a central board.
  • Efficient and timely reviews
    • IRB meetings twice weekly.
    • Expedited IRB reviews on a daily basis.
    • Notification of IRB decisions within 2 days of the meeting and 5 days for formal communication.
  • Comprehensive audit processes
    • Protected class and recombinant DNA/gene transfer trials audited for compliance as part of our routine service.
    • Every investigator new to clinical research is audited to assess GCP compliance.
    • BRANY QA Auditors work with the staff on-site, making the audit an educational experience.
  • Clear communication and accessibility
    • We provide immediate feedback and clear communication on documents submitted to our IRB, including providing redlined recommendations.
    • Access to IRB-Manager™ collaborative software.
    • Emergency contact 24/7.

For more information on BRANY’s Central IRB Services contact Carmela Houston-Henry at 516-470-6979 or choustonhen@brany.com