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13 Dec 2022 | 10:00 AM GMT

Masterclass: Future EU Regulations for AI in Medical Devices

Anchored by:

Erik Vollebregt
Partner
AXON LAWYERS

Participants:

Erik Vollebregt PartnerAxon Lawyers
Erik Vollebregt
PartnerAxon Lawyers
Tessy Huss Director of Strategy , HLTH CommunityHLTH Community
Tessy Huss
Director of Strategy , HLTH CommunityHLTH Community
Ashutosh Malhotra Director Digital Health Strategy & PartnersDaiichi Sankyo
Ashutosh Malhotra
Director Digital Health Strategy & PartnersDaiichi Sankyo
Dr. Nick (Nemanja) Kovacev Head of Healthcare and Life Sciences PracticeHTEC Group
Dr. Nick (Nemanja) Kovacev
Head of Healthcare and Life Sciences PracticeHTEC Group
Ekta Foster-Lachmandas Digital Health Business CreationRoche Diagnostics
Ekta Foster-Lachmandas
Digital Health Business CreationRoche Diagnostics
Jorge Juan Fernández García Chief Innovation OfficerHospital Clínic Barcelona
Jorge Juan Fernández García
Chief Innovation OfficerHospital Clínic Barcelona
Keith Grimes CEO & FounderCuristica
Keith Grimes
CEO & FounderCuristica
Muge Ogrunc Strategic Business DeveloperInstitut Pasteur
Muge Ogrunc
Strategic Business DeveloperInstitut Pasteur
Ouriel Barzilay Chief Technology OfficerDermaDetect
Ouriel Barzilay
Chief Technology OfficerDermaDetect
Spencer Jones Executive Director Global Digital Health Bristol Myers Squibb
Spencer Jones
Executive Director Global Digital Health Bristol Myers Squibb

About this Meeting

Each Masterclass is led by an expert anchor in their field as they dive into their specialty topic in front of a small intimate audience of 8-12 participants. Masterclasses also have an interactive element, allowing you a safe space to share your thoughts and experiences as well as pose questions to the expert anchors. 

Are you trying to commercialize AI-based digital health solutions in the European Union (EU)? Would you like to learn practical steps on how to navigate the EU regulations for AI in medical devices? Join us in this masterclass led by Erik Vollebregt (Partner at Axon Lawyers) to learn more about:   

  • Current AI regulation in medical devices as SaMD (Software as a Medical Device) or SiMD (software in a medical device) 
  • What will (likely) change under the proposed EU AI Regulation? 
  • Current status of the AI Regulation's legislative process journey - when will it be adopted and what will it look like by then? 
  • Other relevant EU regulation for medical devices that deploy AI

We would like to remind you that our meetings are small and intimate sessions with a limited number of seats available, therefore we rely on your attendance and participation to ensure a high quality and valuable meeting for all. If you are confirmed for this meeting we ask if you can please ensure your attendance on the day.