Central IRB Services
“Going the extra mile is a big part of our DNA. Personal attention can go a long way in ensuring the success of your next research study.”
Raffaella Hart, MS, CIP
Sr. Vice President, IRB and IBC Services
Fast, reliable IRB review for multisite studies backed by expert oversight and responsive support. With streamlined submissions, frequent meetings, and dedicated client managers, BRANY IRB helps you save time and money while maintaining full regulatory compliance.
BRANY IRB provides pharma, biotech and medical device companies with Central IRB Services that combine our service-first philosophy, our expertise and a proven, efficient process.
Central IRB Review That Adapts to Your Needs
With BRANY IRB in your corner, you’ll have a team of experts you can count on. Our collaborative approach means we can provide you with the ultimate flexibility. You are never just a number with us. If you have a question about IRB review or the submission process, we will take the time to make it crystal clear. No project is too big or task too small.
With BRANY Central IRB Services, you’ll get
- Competitive pricing
- Collaborative teamwork
- Solution flexibility
- Expert committee and IRB staff
Protocol Review Expertise in All Therapeutic Areas
Our experienced IRB leadership, administrators and committee members are committed to providing the highest quality ethical review. We provide expertise in all therapeutic areas, including but not limited to:
- Gene Transfer
- Rare Diseases
- Oncology
- Cardiology
- Medical Devices
- Pediatrics
- Digital Health
- Neurology
A Proven Central IRB Review Process
At BRANY IRB, we work the way that works for you. Here’s what you can expect when you partner with us:
Easy Submission
Submitting your documents, making amendments, and continuous reviews are all simple with IRBManager™.
The platform is designed for a short learning curve, and all training, instruction sheets, tutorial videos, and one-on-one sessions are included
Frequent Meetings
Our IRB meets daily to ensure IRB review timelines align with your study timeline.
Daily expedited reviews ensure urgent submissions are addressed quickly and efficiently.
Fast Turnaround Times
Receive feedback or answers to questions within 24 hours, keeping communication clear and consistent.
Once the IRB’s questions or conditions are addressed, written approvals and expedited review decisions are delivered within 48 hours to maintain study momentum.
Dedicated Client Managers
You will be paired with a dedicated project manager who understands the details of your studies and timelines.
This personalized support ensures smooth coordination and responsive communication throughout the trial.
Expert Committee & IRB Staff
Representation on our IRB committee includes thought leaders from a wide range of therapeutic areas with diverse backgrounds and decades of experience as IRB members.
Our founders and current owners are the top academic medical centers in the New York City area, giving us the ability to bring together leading clinical and allied health professionals as members on our IRB committee. Additionally, BRANY IRB leadership and staff include Certified IRB Professionals, legal experts, and research professionals, many with more than 10 years of experience in IRB administration.
IRBManagerTM online software
Our web-based IRB management system streamlines the entire review process, from submission to approval. Using IRBManager™ forms, you are guided to provide complete and accurate information, while automatic email alerts keep you updated at every step. All submissions, policies, and determination letters are securely stored in one place, making it easy to track progress and access essential documents anytime.
Full AAHRPP Accreditation & Experience
We have full AAHRPP accreditation, which was granted in 2006. We also have over 20 years of experience serving as an IRB resource for pharma, biotech, and medical device companies.
IBC Services
In addition to Central IRB review, we offer IBC services to expedite recombinant DNA and human gene transfer studies while ensuring rigorous biosafety oversight. Our team of biosafety experts coordinates IBC and IRB reviews when appropriate, streamlining study initiation and reducing administrative burden for sponsors and sites.
“The staff is outstanding. You are still speaking with a human and, nowadays, you can’t take that for granted.”
– Associate Director for Large CRO
Partner with a Central IRB That Works the Way You Do
At BRANY IRB, we make the review process simpler, faster, and more predictable. Our collaborative approach removes obstacles, adapts to your needs, and keeps your study on track. When it comes to expert Central IRB services, partner with the team trusted by leading sponsors and institutions nationwide.