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.
We have offices in Europe, UK, and Australia, which allows us to conduct
international multi-site clinical trials, while providing local support.
We can help you determine what evidence you need to gather in order to have a successfully launch of your product.