Eclevar MedTech is a global CRO, headquartered in France. We support medical device and IVD manufacturers with the transition to the EU MDR and IVDR by offering following services: clinical evaluation, premarket clinical trials, Post-Market Clinical Follow-up (PMCF) studies, collection of real-life data (RWD) and use of real-world evidence (RWE) to support regulatory submissions.

Eclevar UK seeks to not only support with transition for the EU regulations but to expand its support to the UK regulations both current and new frameworks.

We have offices in Europe, UK, and Australia, which allows us to conduct international multi-site clinical trials, while providing local support.