France Local Networking Group Virtual Event: Placing a Medical Device on the French Market : Get the

By nature EU medical devices and in vitro diagnostics regulations aim to improve harmonized regulatory practises within EU member states. However, in certain areas, in accordance with the principle of subsidiarity set out in the Treaty on European Union, there are still national specificities that go beyond the national language requirements that we can obviously think of.

Join us to find out more about the specificities of the French context, such as advertising, vigilance, maintenance, and rules for the disinfection and sterilisation of reusable devices in health care facilities.

Registration Fees & Deadlines

Speakers

Thierry Sirdey
Team Lead Innovation and Operational Excellence, ProductLifeGroup

Corinne Delorme
Regulatory Intelligence Director, Nexialist

Platinum Chapter Sponsors 

MDSS 

RxTROSPECT

Cancellations and Refunds

RAPS reserves the right to cancel this program at its sole discretion. RAPS will not be responsible for travel or other costs incurred due to cancellation. All cancellation requests must be submitted in writing to support@raps.org. Cancellations will receive a full refund minus a 20% administrative fee. RAPS is unable to accept cancellations by phone.

Substitutions

Paid registration substitutions may be accepted with written approval from RAPS for requests received before the start of the event. To transfer a registration, email support@raps.org with the event title, name of the original registrant and the contact information for the new attendee.

Proof of Attendance

A certificate of attendance can be downloaded from the RAPS Learning Portal following the event.

Questions