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.
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VISIT US
ECLEVAR FRANCE:
231 rue Saint-Honoré, 75001 Paris, France
ECLEVAR GMBH
ERFURT, Erfurt Hauptbahnhof
4th, 5th floor
Bahnhofstr. 38 Erfurt 99084
ECLEVAR Australia
Umina Beach NSW 2257, Australia
ECLEVAR UK Limited
3rd Floor 207 Regent Street, London, W1B 3HH
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