Event Details

Understanding Europe's Medical Device Regulation


Effective May 26th 2021, the European Union Medical Device Regulation (MDR) governing market access to the European market, is the most significant regulatory change in over 20 years. With the recommended directives under the MDR, there is an important global shift towards traceability, transparency, and post-approval maintenance of medical devices to ensure the highest possible standard in this safety-critical industry.

Join us for a webinar on 24 Jun to discuss the expected regulatory reciprocities in Asia (e.g. Singapore has recently published rafted UDI guidelines), the impact of such requirements on mid-size/smaller industry players, and how the MedTech industry can leverage this "new era" of transparency in the public-private value chains.

Jun 24, 2021

3:30 PM - 4:30 PM (GMT+8)

Speakers

  • Alex Budiman (Vice President of Regulatory Affairs, Greater Asia at BD)

    Alex Budiman

    Vice President of Regulatory Affairs, Greater Asia at BD

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  • Matt Connors (Director of Operations, International R&D at Genesis Medtech International)

    Matt Connors

    Director of Operations, International R&D at Genesis Medtech International

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  • Diana Hohage (Senior Legal & Compliance Officer at qtec EuRep GmbH)

    Diana Hohage

    Senior Legal & Compliance Officer at qtec EuRep GmbH

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  • Chris Hardesty (Moderator) (Director, Healthcare & Life Sciences Practice of KPMG)

    Chris Hardesty (Moderator)

    Director, Healthcare & Life Sciences Practice of KPMG

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