Think BRANY | IRB and Clinical Trials

Work with BRANY The IRB that

THINKS AHEAD

Start Your Study On a

A successful clinical trial starts with an efficient protocol review.

With deep roots in academic research and clinical medicine, BRANY IRB is uniquely positioned to meet your cost and speed requirements. Get your clinical trial to the start line while ensuring participant health and safety.

Think BRANY for your study.

Easy submission system

Hands-on revisions to your informed consent

Efficient site approvals

Refreshingly responsive support team

Solid Foundation

600+
Institutions

13K+
Contracts & Budgets Negotiated

26 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

Reviewing Protocols Across Therapeutic Areas Since 1998

For over 25 years, BRANY IRB has been a trusted partner for sponsors and CROs running multi-site research studies. We not only provide a high quality review but also go above and beyond in the mission to protect research participants.

Rare diseases
Oncology
Pediatrics

Gene transfer
Digital health
And more

Company ownership

Independent and well-established with roots in academic research and a 25 year history reviewing industry sponsored research

Technology

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

Assists with centralizing training certificates, conflict of interest and other approvals as needed

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

Self evaluates the submission and review processes 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.

Timelines That Meet Industry Standards.
Service That Exceeds Them.

Support Call with a  BRANY Rep

Short Learning Curve for Submission System

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