
Multicenter trials built for coordinated execution across sites
DVCR manages complex multicenter trials in patient populations and healthy volunteers with integrated CRO services, strategic site partners and operational oversight.
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A coordinated model for multicenter study delivery
Multicenter trials require more than site coverage. We support sponsors through site feasibility and selection, external site management, central laboratory services, document workflows and cross-functional CRO oversight designed to keep sites aligned and studies moving.
Strategic site network
We maintain a network of strategic site partners with diverse capabilities and patient populations to support Phase I-III multicenter clinical studies.
Site feasibility and selection
A comprehensive feasibility and selection process helps identify capable sites that align with study needs, sponsor expectations and our execution standards.
Flexibility and responsiveness
We provide sites with clear communication, practical support and essential tools to help reduce friction throughout startup, activation and conduct.
Timely site payments
We carefully coordinate site contracts, monitoring visit documentation, invoice review and payment processing to ensure sites are paid promptly and accurately.
Central laboratory support
Our Central Laboratory Services support standardized processes, centralized testing, real-time data integration, customizable kits, next-day turnaround and dedicated site support.
Site support and communication
Participating sites receive the essential tools, study information, and ongoing support needed for efficient study conduct.
Experience across key therapeutic areas
We support multicenter trials across a diverse range of therapeutic areas and study designs through our CRO services and strategic site partner network.
- CNS, psychiatry & neurology
- Substance use disorders & addiction
- Tobacco harm reduction
- Allergy & immunology
- Cardiometabolic & obesity
- Pain
- Respiratory
- Dermatology
- Infectious diseases & vaccines