External IRB Services for Hospitals/Academic Medical Centers
- We specialize in working with hospitals with in-house research programs seeking to reduce cost and risk by utilizing external IRB services.
- BRANY's IRB can also supplement an existing IRB, replace an IRB that is back logged, or serve as a primary IRB for institutions new to clinical research
- Our IRB is administered by experts in clinical research and human subject protection
- Our unique value proposition:
- Staff from leading academic centers serve as IRB members.
- We combine the expertise of academics with the efficiency of a central board.
- IRB meetings twice weekly.
- Daily IRB reviews.
- All 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, at no extra charge.
- Auditors train the staff on-site, making the audit an educational experience.
- Notification of IRB decisions within 2 days of the meeting.
- We provide immediate feedback and clear communication on documents submitted to our IRB, including providing redlined recommendations.
- Access to IRB-Manager collaborative software.
- Emergency contac 24/7.
For more information about BRANY IRB Services contact Rich Green at 215-327-4919 or rgreen@brany.com
