Everything you need to get IRB approval for your research efficiently and with less frustration.
BRANY Digital Health Toolkit
Efficiently navigate the planning, preparation, protocol writing and IRB submission with our expert services and time-saving tools.
Work with the expert staff and committee members of BRANY IRB. With over 8,500 IRB reviews since 1998, we have the expertise in digital health research – including medical devices and social behavioral research – to ensure an accurate risk and compliance assessment. Get support from our team through the process of preparing for the IRB submission and, if needed, FDA review.
Research Ethics Training
Meet your Human Subject Research requirements with CITI Program, the premier provider of research ethics training. With CITI Program, a BRANY company, you can quickly fulfill the course requirement as well as receive the certificate needed for IRB submission.
Protocol Writing Software
Write your required protocol more efficiently with Protocol Builder, our proprietary cloud-based protocol writing software. Start out with the appropriate template for your research, and get guidance as you go writing your protocol.
Book an appointment with an IRB Expert and learn about our Digital Health IRB Toolkit.