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MedTech Summit
Hybrid Event, 20 - 24 June 2022
In-Person: Clayton Hotel Burlington Road, Dublin, IrelandDigital Experience: One track will be live-streamed each day in BST time zone, with on-demand recording access for all other tracks made available from Monday 27th June. Learn more on the Digital Experience page.

Eclevar MedTech

Profile

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.

Our team

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

We're bringing you

  • A Regulators Perspective on Clinical Evaluations and Investigations

    09:10
  • Case Study : Re-Certification of a Long Term Established Legacy Devices in Ophthalmology under MDR

    14:10