What is sufficient clinical data ?

We are glad to host the first ECLEVAR International Conference on Medical Device which will be organized in Paris. This conference will focus on several topics about the introduction of EU MDR and its impact on clinical evaluation, pre-market clinical trials and post market clinical follow-up. Several speakers from notified bodies to medical device companies will  discuss about the upcoming changes in Medical Device guidelines. This one day conference topics will include :

  – What is sufficient clinical data?, Matthias Fink, TÜV SÜD

  – IVDR, the challenge of clinical evidence requirements, Andreas Stange, TÜV SÜD

  – Real World Data and Clinical Data Solution, Alexandre Templier and Frederic Couriol, ECLEVAR

  – Industry perspective on MDR implementation, Henk Snyman, COOK MEDICAL

  – Digital Clinical Data, Tobias Schreiegg, SIEMENS HEALTHINEERS

  – Clinical Evaluation Report, Dona Occhipinti, HILLROM

  – Automated Clinical Evaluation Report, Chems Hachani and Sébastien Tourlet, ECLEVAR 

Informations about this events will be frequently updated, and the address and date of this conference will also be quickly confirmed. For more information, please contact : 


Andreas Stange

Vice President, TÜV SÜD

Matthias Fink

Clinical Reviewer, Clinical Centre of Excellence, TÜV SÜD

Tobias Schreiegg

Director Regulatory Affairs, SIEMENS HEALTHINEERS

Henk Snyman

Director Regulatory Affairs, COOK MEDICAL

Dona Occhipinti

EU MDR Clinical Evaluation Lead, HILLROM

Alexandre Templier

Lead Human Data Science, ECLEVAR
Co-Founder, QUINTEN

Sébastien Tourlet

Director Strategic Innovation, ECLEVAR

Frederic Couriol

Senior Director, Real World Data Science, ECLEVAR

Chems Hachani

CEO & Chairman, ECLEVAR


Contact :