Webinar: Tackle MDR requirements with your supplier's material expertise

On March 23, at 6 pm Central European Time (CET)/ 1 pm Eastern Daylight Time (EDT) and March 25, at 2 pm CET/ 9 am EDT, Trelleborg Healthcare & Medical will be hosting a free-to-attend webinar.

Tackle MDR Requirements with your Supplier´s Material Expertise.

>> Register now to reserve your seat at the webinar

 

Attend this webinar to:

  • 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

 

Medical Device Regulations

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 because it imposes strict requirements surrounding the approval process and the time and effort needed to bring new devices to market.

Next to an extensive conformity assessment procedure and extended clinical studies, materials and substances are also a focus of the MDR. Special attention is given to the elimination of carcinogenic, mutagenic, reprotoxic (CMR) substances or endocrine disruptors in medical device materials, in order to fulfill MDR requirements. 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.

 

>> Register now for the webinar

>> Contact us to discuss meeting MDR requirements for your medical device designs