Operational services that help sponsors, CROs, and sites move from planning into activation.
Service overview
Startup services focused on faster site activation.
Trial Startup provides specialized support across the activities that shape clinical trial startup timelines in Europe, from early feasibility through submissions, contracts, and essential documents.
Feasibility, evaluation, visits, document collection, submissions, contracts, and startup tracking.
Site selection and feasibility
Build a realistic site and country strategy before startup activities fragment across teams.
Site feasibility and evaluation
Understand site fit, readiness, responsiveness, and practical activation risk before activation.
Site evaluation visits
Use structured visits to validate site fit, local processes, and early operational readiness.
Document collection
Coordinate document requests, follow-up, review, and package completeness before submissions.
Regulatory authority submissions
Organize competent authority submissions and follow-up across European country pathways.
Ethics committee submissions
Prepare and progress ethics submissions with tighter ownership and cleaner document flow.
Budget and contract negotiations
Drive budget alignment and study contract discussions without losing track of activation timelines.
Essential documents
Keep startup documentation complete, current, and structured around what activation requires.
Study startup management
Coordinate milestones, escalations, reporting, and cross-functional actions through startup.
Contact
Need a startup partner across Europe?
Trial Startup provides practical, focused support across the operational work that drives activation.
Country focus