KEY INSIGHTS ON EU MDR RECENT AMENDMENTS AND THEIR IMPLICATIONS

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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

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