Tackle MDR requirements with your supplier's material expertise
Key takeaways of the webinar include:
- Gain an understanding about MDR material related requirements
- Learn how a partner-like approach helps you identify and fulfil these demands
- Discuss requirements and solution approaches with Trelleborg experts
The EU medical device regulation (MDR) 2017/745 was announced five years ago and will fully apply on May 26, 2021. The new MDR poses major challenges for medical device manufacturers. Through close cooperation, suppliers can support medical device manufacturers in complying with these requirements.
Webinar Presenters:
Our keynote speaker, Stefan Bolleininger from be-on-quality, understands the requirements from a supplier’s point of view and will share insights into these and the necessary testing process to ensure compliance with MDR.
Trelleborg Healthcare & Medical experts, Verena Hörner and Andreas Schmiedel, will take an in-depth look at the Trelleborg MDR strategy and the support provided to medical device manufacturers in meeting MDR material-related requirements, as well as the connection to standards like ISO 10993.