Preparing Technical Documentation for Medical Device Regulation

Join our webinar to learn why you should have technical documentation and what needs to be considered to establish compliance.

We will discuss important elements that need to be taken into account when creating the technical documentation, but will not go into specific details of each requirement. We will, however, give some key points and explain how Notified Bodies are looking at your technical documentation.

Target Audience

This webinar is aimed at medical device manufacturers.

Speaker

Virginie Siloret
Global Medical Device Certification Manager
SGS

Date/Time: Wednesday, July 13, 2022, at 9:00 am EDT

For further information, please contact:

Victoria Leo
Marketing Specialist
t: +1 201 508 3000