Our Rapid Trial Activation service provides sites/institutions with a specialized team of seasoned clinical trial site subject matter experts who lead, coordinate, and manage the end-to-end startup process for clinical trials. This service encompasses end-to-end trial start-up support, including regulatory and IRB submissions in collaboration with Sponsors and CROs, budget negotiations and coverage analysis, contract execution, CTMS configuration, pharmacy setup, protocol training, and overall site readiness. Our goal is to accelerate recruitment timelines, optimize enrollment potential, and enhance the site's return on investment.

For Sponsors and CROs, this service accelerates timelines to first patient in (FPI) by streamlining site onboarding, enhancing trial efficiency, and helping ensure studies stay aligned with projected milestones.

For Sites, it accelerates trial initiation by simplifying administrative processes, reducing operational burden, and shortening time to activation.