MDR and the impact on chemical substances in Medical Products

The new Medical Device Regulation 2017/745 (MDR) fully applies since May 26th, 2021. The entry into force not only changes the requirements of the documentation and certification procedure, but also the requirement of hazardous substances. TÜV Rheinland is one of the few Notified Bodies accredited under both MDR and IVDR regulations. 
We invite you to join our webinar "MDR and the Impact on Chemical Substances in Medical Products” where our expert will provide an overview of the changes for hazardous substances, the challenges for the risk assessment and examples of test including typical results.
Webinar Outline:

  • Overview of the changes about hazardous substances
  • Impact on the risk assessment
  • Examples of substances discovered in Medical Devices
  • Preparing for an audit in regards of hazardous substances

Choose your session

Date
Time
Time zone
Speaker
Language
October 26, 2021 [Session 1]
10.00 am
[Berlin, 1 hour]
[Beijing, China] 4:00 pm
[Berlin, Germany] 10:00 am
Nina Marx & Geoffrey Bock
English
October 26, 2021 [Session 2]
6.00 pm
[Berlin, 1 hour]
[Berlin, Germany] 6:00 pm
[New York, USA] 12:00 pm/Noon
[Los Angeles, USA] 9:00 am
Nina Marx & Geoffrey Bock
English

Our Experts

Our Expert: Geoffrey Bock

Geoffrey Bock has managed hazardous chemicals in products for the last 15 years at TÜV Rheinland. Currently, he is developing sales and educating customers on chemical product requirements.
Our Moderator: Nina Marx

Nina Marx studied Medical-Economics in Cologne, Germany and is part of the medical device sales team for 13 years. She cares a lot for services for audits of medical device manufacturers, but her focus has always been on the testing and certification of medical devices.
Your Registration:

By registering for our webinar, you confirm receiving confirmation, reminder and follow-up emails of the event, including documents and/or presentations and contacted by the sales representatives on the webinar topics in the future. In return for the webinar information, we only ask for your e-mail address and your consent that we may continue to send you regular information about TÜV Rheinland products and news by e-mail in the future.
The fields marked with an * are mandatory fields.




© TÜV Rheinland 2024
 
Back to top