Authorized Representative Services
Live Webinar
April 30, 2020
Book now our live webinar and see the MDR presented with a different flavor - the EC REP perspective on the MDR!
Exchange views and experiences in a classroom style interaction from your home office environment.
The "NEW CE MARKING"
- Economic Operators -
Covering the MDR Delay and learning why your Importer may require MDR compliant products already today!
Date: April 30, 2020Time: 6pm Central Europe / 12:00 PM - Eastern / 09:00 AM - West CoastWith the European Medical Devices Regulation 2017/745 (MDR) taking effect in May 2021 (1 year delay), it is important to understand the particular aspects the manufacturer must address today for the "NEW CE MARKING” and recognize the impact of the new legal concepts for the Importer and Distributors.The 12 month delay is just a short period considering that the Importer will now request MDR compliant products.
|
Join us and let us guide you in these turbulent times.
| Since 2000 President Medical Device Safety Service GmbH (MDSS) Founder MDSS Consulting and ITN Holding GmbH 1996-2000 Lead Auditor and Expert with leading Notified Body (TÜV Rheinland) 1997-2000 Manager of the San Diego TUV office 1995-1996 Research and Development of Medical Devices University degree (Dipl. Engineer), Aachen University of Technology Member and Deputy Chair of the European Association of Authorized Representatives (EAAR) Member of the European Medical Device Coordination Group (MDCG) and the Commission Working Group on Vigilance. Member of the Ethics Committee of the Medical Council (Aerztekammer) for Lower Saxony Member of the Regulatory Affairs Professional Society (RAPS) Founder and President of the RAPS Germany Chapter | Presenter  Ludger Moeller MDSS President |
Book this webinar for your company and have your specific needs and internal sensitive topics addressed.
Pick a date of your choice and have all your questions answered!
Webinars will be offered via Zoom
