Independent IRB, compliance, monitoring and auditing for clinical trials
Services for Hospitals/IRBs
BRANY was founded by the country’s leading academic medical centers in 1998, and has a stellar track record of working with community and academic hospitals and established investigators. BRANY understands the importance of high quality human subject research. In today’s increasingly complex study environment, we excel in helping IRB’s and hospitals continue to provide their patients with high quality clinical research. BRANY offers personalized customer service and project management, as well as ongoing communication through our quarterly newsletter and regular email updates.
BRANY’s “connected IRB” model provides institutions with a customized solution that results in high quality human subject protection oversight, as well as efficiency for industry sponsored and investigator-initated research.
Our team of experts offers comprehensive eligibility review for your clinical trials to determine if they meet the requirements of Medicare’s clinical trial and device policies.
BRANY can help identify clinical research opportunities that match investigators’ research interests and expertise.
Investigators benefit from BRANY certification with increased access to research opportunities and visibility to sponsors.
With our Smart-Start-60 program, we can initiate clinical trials within 60 days at any of our certified investigator sites.
Well-versed in FDA regulations and GCP guidelines, our monitors will provide the highest quality oversight of your research study.
Our expert consultants can play an instrumental role in the successful realization of full three-year accreditations.
Our core committee is composed of chairs and biosafety officers from academic medical centers.
BRANY’s clinical research compliance program promotes operational excellence, best practices, and regulatory compliance.