Thinking Ahead with TÜV SÜD Podcast

KEY INSIGHTS ON EU MDR RECENT AMENDMENTS AND THEIR IMPLICATIONS

Powering the Future with TÜV SÜD: Episode #7

Powering the Future with TÜV SÜD: Episode #7

Powering the future V-Blog

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ABOUT THIS EPISODE

While placing their products in the European market, one of the primary requirements for medical device manufacturers is the implementation of European Medical Device Regulations (EU MDR) and ensuring compliance towards the EU MDR for getting the Conformité Européene (CE) markings on the products.
In this podcast, Dr. Anita Joshi, who holds a PhD degree in Biotechnology from the National Institute of Virology India shares key insights with regards to the latest amendments in EU MDR regulation.


EU MDR PODCAST OVERVIEW

  • 01 min 20sec - Introduction
  • 02 min 21 sec - Why did the new regulation come into place?
  • 04 min 22 sec - What changes does the new regulation bring?
  • 06 min 52 sec - What are the conditions for benefiting from the new regulation?
  • 07 min 41 sec - Why should manufacturers know about this amendment?


RELATED LINKS

For more information about our EU MDR 2017/745 training program, visit EU MDR- Implementation and Advanced Requirements for EU MDR 2017/745 - with free e-learning

 

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