Calling on Medical Device Enthusiasts of the European Regulatory Framework
The GMED NA Forum is an exciting and engaging learning opportunity with presentations, workshops and roundtables focused on the EU MDR 2017/745 and IVDR 2017/746. The forum will take place on:
Monday, November 18th, 8:00 am - 6:30 pm, in Palo Alto, CA.
The new European Regulatory Framework has tremendous economic and practical challenges for Medical Device Manufacturers. With deadlines looming, companies need to understand the new Framework and their implications.
This forum will give you an opportunity to speak with Medical Device Certification Experts who will answer your questions and help you assess your readiness level for implementing the (EU) 2017/745 and/or (EU) 2017/746.
Key topics include:
Article 120 & 110 Implementation;
Transition to EU Regulations 2017/745 (MDR) & 2017/746 (IVDR);
Clinical evaluation under the aegis of the new Regulation (EU) 2017/745 on Medical Devices;
Medical Device Usability - Latest Standards and European Requirements;
Fully owned subsidiary of GMED SAS. • GMED, Notified Body n° 0459
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