MedFIT organises a NEW activity entitled Meet-the-Experts sessions where participants can adress their specific needs to medtech experts. Participants, it’s time to book a meeting with our medtech experts!

The Experts:

  Cyrille Michaud

QA/RA, CE/FDA, SOFTWARE MEDICAL DEVICE LIFE CYCLE MANAGEMENT

 Sébastien Ferret

CLINICAL EVALUATION, RISK MANAGEMENT, REGULATORY STRATEGY, CE-MARKING

  Christine Horvais

HR AUDITS, EVALUATION INTERVIEWS, RECRUITMENT IN SALES-MARKETING-QA/RA-CLINICAL STUDIES-R&D-TOP MANAGEMENT

  Mathieu Charleux

INTERNATIONAL BUSINESS DEVELOPMENT AND STRATEGY

  Emmanuelle Dura-Badez

CLINICAL EVALUATION, LITERATURE REVIEW, CLINICAL STUDIES, REGULATORY FILING

   Julien Prouteau

QMS ISO13485, CE-MARKING, PROCESS VALIDATION

  Christine Grasset

PRODUCT DEVELOPMENT, FUNDING INNOVATION

  Alain Valorge

ISO13485:2016, NEW MDR 2017/745, CE, 510(K), STED, AMDEC, AUDITS…

  Eric Filion

QA/RA, FDA CLEARANCE, MDSAP, CANADA, USA, NORTH AMERICA, SALES SUPPORT

Log in to the partnering platform to request a meeting*

*Only MedFIT registrants can login to the partnering platform. Haven’t yet registered? Book now!