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ON-DEMAND WEBINAR

ON-DEMAND WEBINAR

A delay in MDR? Where are we now?

Published Date: December 10, 2020

With the COVID-19 crisis, the Medical Device Regulations (MDR) have been pushed back one year, this delay has given a respite for those companies that were not quite ready for the increase regulations. In this talk we will be discussing the current status of the medical device industry regarding MDR and what are others doing to get ready. Attendees will learn:

  • What additional requirements are in the MDR?
  • Where is the industry currently at and how many companies feel ready for their first submission?
  • What have we learned from the first submissions under MDR?
  • What are others doing now, to save time and money?
Thor Rollins

Thor Rollins

BS, RM (NRCM)
Toxicology and E&L Expert

Thor Rollins is a certified microbiologist and specializes in the selection and conduct of in vitro and in vivo biocompatibility tests. He actively speaks on biocompatibility related topics through Nelson Labs’ external seminars, webinars, and tradeshows. He presented on biocompatibility at the American College of Toxicology annual meeting in 2013 and has published many articles...

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