Uncovering the MDR key changes made easy by DNV GL
On 5th April 2017, the European Parliament voted to adopt the long-awaited Medical Dev ice Regulation (MDR)
The MDR regulation will replace the current medical device directive (MDD) and the active implantable medical device directive (AIMD).
In this seminar, we have focused on key changes of MDR and Transition Period.
These are the topics being covered:
- The New Medical Device Regulations
- Transition to MDR
- Key changes
- MDR Annexes
- Steps manufacturers should take now and how DNV GL can help
Our first Collaboration with Federation of Malaysian Manufacturers was successful. We have gathered about 40 attendees from the Medical device manufacturers industry and has reached out to senior positions in each organisation. Our presenter, Mr Hasan Zarin Mehr (Lead Auditor/ MDD Accessor) has given our delegates insights into how they could cope with the changes in the regulation. The seminar was interactive and our delegates have given very positive feedback about our seminar.
If you would like to have a copy of what was being presented during our seminar, you may download a copy here.
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