Trial roadmap

Clinical trial roadmap.
Progress step by step.

Upfront we work with all clients to clearly identify project goals, priorities, budgets, and timelines to customize a solution  for your needs.

Meditrial Europe delivers a well-coordinated, collaborative approach that is critical to every phase of clinical trials – from writing protocols, maintaining essential documents, preparing informed consents and translations, to compiling initial submissions, amendment, notifications and closeout reports. We constantly collaborate with regulatory authorities and ethics committees.

Using our standard operating procedures, dedicated clinical specialists oversee activities throughout the study. We rigorously track metrics to ensure timelines for study start-up are met.

Every country and site are different, and Meditrial’s submissions teams have extensive experience in the execution of multiple Clinical Trial Agreements with sites, investigators, and core laboratories.

Our client password protected system enables live access to complete study files and documentation.  Each project manager has complete control of the study dossiers, approvals, monitoring reports and much more.