On 5th April 2017, the European Parliament voted to adopt the long-awaited Medical Device Regulation (MDR)
The MDR regulation will replace the current medical device directive (MDD) and the active implantable medical device directive (AIMD).
In this Webinar, we will focus on key changes of MDR and Transition Period
Key talking points
- Key Changes in New Medical Device Regulation (MDR)
- CE Marking Process
- MDR and Transition Period
This webinar will help you to consider necessary action required to be prepared for the change in requirements of standard as well as planning of CE Marking.
Hasan Zarin Mehr is Lead Auditor/MDD Assessor at DNV GL with more than 12 years. His experience in Medical Device Industry was through his past working as a Medical Device Technical Specialist, QMR/QA and was a consultant and trainer to a wide range of Medical Device manufacturers. He has helped organisations in implementing Quality Management System in accordance with ISO 13485 and provided Technical Documentation for CE Certification in all classes of Is, Im, IIa, IIb and III.
His academic qualifications include a MSc in Biomedical Engineering and a BSc in Biomedical Engineering.