ABOUT BRANY
BRANY IRB is a fully AAHRPP-accredited, independent IRB with deep roots in clinical research and the protection of research participants. With over 25 years of experience, BRANY IRB provides pharmaceutical, biotech and medical device companies with central IRB solutions that combine a service-first philosophy with a proven, efficient IRB review process. BRANY IRB also provides a user-friendly submission management system that simplifies online submissions and provides 24/7 access to all necessary IRB-related documentation.
BRANY IRB brings extensive expertise in central IRB review studies across diverse therapeutic areas, including cell therapy, neurology, oncology, medical devices, and digital health. With a deep understanding of regulatory complexities and ethical considerations, we navigate even the most intricate protocols with precision. Our streamlined review process for multi-site studies supports sponsors and CROs with fast-moving IRB review, accelerating study start-up and advancing critical research. Offering transparent pricing and a commitment to your success, BRANY IRB helps clients, and their sites navigate the IRB process with ease.
FEATURED ARTICLES
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![iStock-528606286-handshake-partnership-partner-agreement]( "Conflict Of Interest: Implications For Clinical Research Sites")
Amid scrutiny of the financial conflicts of interest in biomedical research, new federal rules aim to improve transparency and preserve the integrity of publicly funded research.
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![GettyImages-1370928101 regulatory compliance]( "Is Your Clinical Research Site GCP-Ready?")
Explore a comprehensive overview of Good Clinical Practice (GCP) guidelines. By fostering a culture of continuous improvement through internal audits, clinical research sites can identify non-compliance issues and enhance their research practices.
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![Brain-Power-GettyImages-1130826731]( "Informed Consent In Clinical Trials Involving Neurologic Disorders")
Informed consent is essential in clinical research. However, when participants lose decisional capacity, a Legally Authorized Representative (LAR) is needed to provide consent and uphold ethical standards.
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![GettyImages-1245953899 IRB compliance]( "Initial IRB Submission: 7 Fundamentals Of Success")
This article outlines seven key fundamentals for optimizing IRB submissions and streamlining approvals, keeping their clinical trials on track.
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![GettyImages-1165109678-handshake-partner-business-agreement]( "8 Critical Questions To Ask Your IRB")
This article outlines eight essential questions to ask a potential IRB partner to assess their ability to help you navigate complex regulatory requirements while avoiding delays.
CONTACT INFORMATION
BRANY
1981 Marcus Avenue Suite 210
Lake Success, NY 11042
UNITED STATES
Phone: 516.202.1576
Contact: Robert Whitaker, Director of Client Services for Central IRB
