IRB review, compliance and monitoring for clinical trials and CROs

Services for Sponsors/CROs

BRANY provides comprehensive solutions to Sponsors and CROs for research involving medical devices, biologics, diagnostics and all therapeutic areas. Our services include: Central IRB; site indentification and start-up, monitoring, auditing and compliance; and administrative support. We work with companies of all sizes, including emerging companies with a small clinical staff and limited resources. In today’s increasingly complex study environment, we excel at keeping studies on track and on time.
For more information about IRBs, go to IRB Services.

Central IRB (AAHRPP-Accredited) With Expedited Reviews

Site Identification

“Smart-Start-60”: Guaranteed Site Start-Up Within 60 Days

Monitoring & Auditing Services

Compliance Services

BRANY Certified Sites

Institutional Biosafety Committee Services (IBCs)