This service manages the end-to-end startup process for clinical trials, including budget negotiations/coverage analyses, contract negotiations, IRB submissions, CTMS build-out, protocol training, and Site readiness.

For Sites, it accelerates study initiation by streamlining administrative steps and reducing activation delays.

For Sponsors and CROs, it significantly shortens timelines to first patient in (FPI) and improves trial efficiency through faster Site onboarding.