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!
