EU Symbols Standard For Devices Moves Closer To Being Harmonized
This article was originally published in SRA
The revised text for part 1 of the new European standard on symbols to be used in medical device labeling to convey information about the safe and effective use of products should be available in the third quarter of this year.
You may also be interested in...
Where are the biggest challenges for notified bodies and manufacturers now there is some experience with the MDR, and can the sector manage the new regulatory requirements successfully?
The European Commission has finally published detailed guidance on the EU IVDR’s classification rules. The IVDR’s completely new classification regime means guidance is urgently needed.
Do you know how to avoid the pitfalls when it comes to clinical evidence under the MDR? Or whether evidence gathered outside the US counts? Amie Smirthwaite of Maetrics answers these and other pivotal questions in this third and final part of an interview series with Medtech Insight.