Sponsors
BRANY has ongoing relationships with more than 200 pharmaceutical and biotech companies and CROs. There are Master Clinical Trial Agreements in place with many of these organizations.
With the largest alliance of clinical research sites in the world BRANY offers a unique value proposition for Sponsors through a turnkey solution for expedited site identification and study start-up.
- Trials can be up and running in as little as 4-6 weeks following receipt of request.
- BRANY’s rapid response is because with agency rights we negotiate for our sites and are the single point of contact for all budget and contract negotiations; assist in preparation of start up regulatory document; and the BRANY IRB is the IRB of record.
- We have the key opinion leaders as well as the high enrolling private sights as part of the network. All our sites are vetted by a team here at BRANY.
- Once the trial has begun all trial management is between the sponsor and the site.
IRB Services
- Central/Independent IRB
- Academic IRB Members
- Unique to Brany IRB - all sites audited
- Personalized customer service
- Daily Expedited Reviews
Institutional Biosafety Committee Services (IBCs)
- Local IBCs formed and registered
- Core board of recombinant DNA/gene transfer and biosafety experts from academic centers
- Network of non-affiliated community members
