Is your biological evaluation ready for MDR?

Free webinar

Listen to our experienced biocompatibility experts talk about the requirements for biocompatibility of medical devices that you are expected to fulfil to comply with MDR as well as new requirements in the most recent standards of the ISO 10993 series. 

Content 

  • MDR General Safety and Performance Requirements related to biocompatibility  
  • Most important updates in ISO 10993-1:2018 and ISO 10993-18:2020 

Who should attend: 

Everyone who wants an increased understanding of biocompatibility concepts in general, and/or more knowledge of current regulatory requirements and recent updates in the evaluation methods. 

Register here: https://attendee.gotowebinar.com/register/2032272843913265424

Share
Date & Time
May 11, 2022
14.00 - 14.20 CET
IndustryCombination products, Medical Device
LanguageEnglish
LocationOnline

make an inquiry

In-House Training

This course is available as an In-House Training course. Let us know if you wish to customize a course or if you are a large group with the same requirements.

We take great care of your contact details. To learn more, read our Privacy Policy

Your Instructor(s)

Leading specialist with long experience of training are guiding you through regulations, guidelines, interpretations, requirements and applications.

Emma Pedersen

Emma Pedersen

Search

Cookies

For your best experience are we using cookies on this website.