IRB Services

Work with the IRB that Puts Your
Study First

Start your clinical trial on the right foot with BRANY IRB.

BRANY IRB is uniquely positioned to meet your cost and speed requirements. Talk to our team of IRB experts to learn more about how our team can get your study to the start line while ensuring participant health and safety.

Get in touch to learn more about how we can help with your study.

Easy submission system

Hands-on revisions to your informed consent

Daily IRB meetings

Efficient site approvals

Refreshingly responsive support team

Rapid turnaround times

1000+
Institutions

25+ Years
Reviewing Protocols Across Therapeutic Areas

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

Put 25+ Years of Experience Across
Therapeutic Areas to Work for Your Study

BRANY IRB has been a trusted partner for sponsors and CROs running multi-site research studies. Talk to our experts and learn more about how we provide high-quality reviews and go above and beyond in our mission to protect research participants in all therapeutic areas.

Rare diseases
Oncology
Pediatrics

Gene transfer
Digital health
And more

Company ownership

Independent and well-established, with a 27-year history of reviewing industry-sponsored research

Technology

Owns the technology behind the submission platform, allowing us to be flexible and make improvements based on customer feedback

Allows for multiple related items in one IRB submission

Service

Quickly responds to emails and phone calls to address any questions as soon as possible – including our leadership team

Prescreen the submission to ensure the experience is effective and efficient

Answers questions fast, follows up on feedback, and implements revisions to informed consent post IRB review

I would use BRANY over anyone else. I can ask them anything, even questions on feasibility.
Other IRBs aren’t as hands-on.

– Research Coordinator for Multi-Site Study

GET IN TOUCH

– Associate Director for Large CRO

The staff is outstanding. You are still speaking with a human and, nowadays, you can’t take that for granted.

BRANY IRB screens new submissions rapidly and communicates feedback and questions in advance of IRB meetings. We’ll keep you updated every step of the way.

Independent IRB Timelines That Meet Industry Standards. Service That Exceeds Them.

Support Call with a  BRANY Rep

Easy-to use
Submission System

Daily Meetings & Expedited Reviews

Rapid Feedback & Questions

Post-IRB Meeting
Notification
within 1 day

IRB Submission Technology
Built & Supported by BRANY

The next era of drug development requires the next era of IRB submission technology. Our proprietary submission management system is easy to learn and supported by real people.