Registration will close June 2, 2020 at

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The MedTech industry is one the world's fastest growing industry sectors.


However, along with the incredible speed of development and acceleration there also comes a predictable host of challenges. Coupled with the growing diversity in product make-up and addition of digital technologies, the depth and breadth of regulatory changes can cripple quality and regulatory functions.


AI and digital automation have the potential to support and transform regulatory functions by streamlining and automating processes, allowing MedTech companies to react to change efficiently while avoiding unnecessary risks.


Sign up for this webinar to:

  • Learn how organisations tackle the growing complexity of managing regulatory intelligence on a global scale
  • Explore common challenges/barriers organisations face as try to be more efficient
  • Understand where regulatory intelligence as a process is headed as technology enables a new level of automation & augmentation
  • Take these lessons back to your organisation to mature your own regulatory intelligence program


Date: Wednesday, 3 June 2020

Time: 9am to 10am (Singapore time)


This webinar is conducted in partnership with Clarivate Analytics. Login details will be shared via email with those who have registered for the event, closer to the event date.

Jun 3, 2020

9 AM - 10 AM

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Speakers

  • Teresa Fishburne (Global Practice Lead, Clinical & Regulatory Consulting and Head, Centre of Medicines Research at Clarivate Analytics)

    Teresa Fishburne

    Global Practice Lead, Clinical & Regulatory Consulting and Head, Centre of Medicines Research at Clarivate Analytics

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  • Elizabeth Holloway (Senior Regulatory Solutions Consultant at Clarivate Analytics)

    Elizabeth Holloway

    Senior Regulatory Solutions Consultant at Clarivate Analytics

    Read Bio
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