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Healthcare is one of the industries that have the most to gain from the rise of AI, and the term "going digital" has become more and more synonymous with healthcare.


However, some imminent challenges must be overcome before physicians and other healthcare professionals can fully benefit from a digitised health ecosystem. Regulatory bodies have to re-imagine their approaches to AI regulation to fit the rapid, iterative nature of AI-based solutions. Integrated health data sets must comply with existing privacy laws like the EU's General Data Protection Regulation, and organisations must ensure data protection, transparency and cyber security.


Sign up for this webinar to hear from Nathan Carrington from Roche Diagnostics and Lucas Nicolet-Serra from Simmons + Simmons and better understand what frameworks currently regulate AI and what is preventing the proliferation of AI, from industry and legal perspectives. The webinar will be moderated by Varun Veigas from Roche Diagnostics.


Regulating AI-Based Medical Devices

Date: Thursday, 25th June 2020

Time: 9am to 10:30am (GMT +8)


Please note that this webinar is exclusive to APACMed members only. Login details will be shared via email with those who have registered for the event, closer to the event date.

Jun 25, 2020

9 AM - 10:30 AM

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Speakers

  • Lucas Nicolet-Serra (Supervising Associate at Simmons & Simmons JWS Pte. Ltd)

    Lucas Nicolet-Serra

    Supervising Associate at Simmons & Simmons JWS Pte. Ltd

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  • Nathan A. Carrington (Senior Regulatory Policy Advisor, Global Regulatory Policy and Intelligence at Roche Diagnostics)

    Nathan A. Carrington

    Senior Regulatory Policy Advisor, Global Regulatory Policy and Intelligence at Roche Diagnostics

    Read Bio
  • Varun Veigas (Regional Manager, Regulatory Affairs & Policy, Asia Pacific at Roche Diagnostics)

    Varun Veigas

    Regional Manager, Regulatory Affairs & Policy, Asia Pacific at Roche Diagnostics

    Read Bio
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