Phase I-II Multi-Site Trials

By combining our full suite of CRO support services and a network of strategic site partners globally, we manage complex multi-site trials in patients and healthy normal volunteers across a diverse range of therapeutic areas and trial designs.

Our team has significant experience managing external site activities, including site feasibility and management, for the seamless delivery of high-quality data to our sponsors. We maintain a network of strategic sites that have a diverse range of capabilities and patient populations to conduct multi-site clinical studies. Our comprehensive site feasibility and selection process ensures that the most capable sites participate in your study and align with our commitment to speed, customer service and delivering the cleanest data possible.

WEBINAR ON-DEMAND

The Hidden Risk in Early Development:

Why Programs Lose Momentum

Discover how continuity in project leadership, study management and clinical monitoring influences execution quality, decision confidence and program momentum in early phase development.

Watch the Recording

WEBINAR ON-DEMAND

The Hidden Risk in Early Development:

Why Programs Lose Momentum

Discover how continuity in project leadership, study management and clinical monitoring influences execution quality, decision confidence and program momentum in early phase development.

Watch the Recording

WEBINAR ON-DEMAND

The Hidden Risk in Early Development:

Why Programs Lose Momentum

Watch the Recording

We prioritize sites that align with our principles to help our sponsors reach their milestones faster.

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Site ID and Selection

Quality sites are imperative for a successful trial.

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Prioritizing Site Payments

Sites require expedited payments to avoid study delays. This reinforces our collaborative, true partnership approach.

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Site Engagement

We provide sites with essential tools, support and communication.

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Central Laboratory Services

DVCR’s Central Laboratory streamlines multi-site trials through standardized processes, centralized testing and real-time data integration. We have customizable kits, next-day turnaround times and proactive shipment monitoring. With a single comprehensive Central Lab Manual and dedicated support teams, DVCR reduces site burden and quickly adapts to protocol changes – keeping your study on track from start to finish.

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Florence Trial Operations Platform

The Florence Trial Operations Platform accelerates the study startup and enables seamless document distribution, tracking and remote monitoring across our sites. It provides real-time visibility and quality control, eliminating the need for back-and-forth exchanges and integrates directly with Trial Master Files (TMFs) for efficient filing and document updates. Whether sites
use a Florence account or paper ISF, this tool keeps DVCR connected and informed—especially during critical phases such as startup and site activation.