Date: 24 May 2023
What is the webinar about?
The webinar presents an overview of the MDR Conformity Assessment Routes, the application process and the review approach of BSI, tailored to SMEs in the AIMD space.
Who should attend?
All SMEs who intend to apply for CE marking under the Medical Device Regulation. Manufacturers interested in gaining a better understanding of MDR Conformity Assessment Routes are also welcomed to join.
What will participants gain?
We will talk about the classification of devices including accessories, points to consider in preparing a comprehensive technical documentation package and provide general lessons learnt about review timelines and associated service levels BSI can offer.