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Masterclass: Future EU Regulations for AI in Medical Devices

13th December @ 10AM GMT / 6PM AWST

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.

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Masterclass: Future EU Regulations for AI in Medical Devices

Erik Vollebregt
Partner, Axon Lawyers
Ekta Foster Lachmandas
Digital Health Innovation & Business Creation with the Roche Startup Creasphere
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Masterclass: Future EU Regulations for AI in Medical Devices

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Participate in this Digital Health Sprint in order to:
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Don't miss your opportunity to connect with senior leaders to shape the future of digital health. Because only if you are prepared now can you lead the future.

13th December @ 10AM GMT / 6PM AWST

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.

Apply to AttendRegister to AttendApply to Attend

Participants

Participants

Erik Vollebregt

Partner, Axon Lawyers

Ekta Foster Lachmandas

Digital Health Innovation & Business Creation with the Roche Startup Creasphere

Müge Ogrunc

Entrepreneur In Residence, Antler

Nemanja (Nick) Kovačev

MedTech Expert, HTEC Group

Ashutosh Malhotra

Digital Business Development & Innovation Scouting Manager Europe at Daiichi Sankyo Europe GmbH

Tim Jurgens

Co-Founder & General Manager en SeedLink SL

Keith Grimes

Primary Care Physician, Digital Health & Innovation Consultant, and Founder of Curistica

Marie-Noel Achkar

Head of DCTx Incubator Operations, UCB

Ouriel Barzilay

CTO, DermaDetect

Dr. Christina Biermann

Head Application Development & Integration, Bayer Pharmaceuticals

Spencer Jones

Digital Health Lead Global Drug Development, Oncology, BMS

Jorge Juan Fernández García

Director of Innovation, EIT Health

Jennifer McCormack

Connected Health Skillnet Manager, IBEC

Number of Participants


Up to 12
Date  
December 13, 2022
Community

Masterclass: Future EU Regulations for AI in Medical Devices

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.

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Set up a free HealthXL platform account for a taste of what the community has to offer. Or talk to us about upgrading to a premium account:

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  • Join specialised communities in areas like DTx, AI, Clinical Trials Innovation and more
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Masterclass: Future EU Regulations for AI in Medical Devices

13th December @ 10AM GMT / 6PM AWST
Digital Therapeutics (DTx)

Masterclass: Future EU Regulations for AI in Medical Devices

13th December @ 10AM GMT / 6PM AWST
Digital Therapeutics (DTx)
Erik Vollebregt
Partner, Axon Lawyers
LinkedIn Profile
Ekta Foster Lachmandas
Digital Health Innovation & Business Creation with the Roche Startup Creasphere
LinkedIn Profile
Müge Ogrunc
Entrepreneur In Residence, Antler
LinkedIn Profile
Nemanja (Nick) Kovačev
MedTech Expert, HTEC Group
LinkedIn Profile
Ashutosh Malhotra
Digital Business Development & Innovation Scouting Manager Europe at Daiichi Sankyo Europe GmbH
LinkedIn Profile
Tim Jurgens
Co-Founder & General Manager en SeedLink SL
LinkedIn Profile
Keith Grimes
Primary Care Physician, Digital Health & Innovation Consultant, and Founder of Curistica
LinkedIn Profile
Marie-Noel Achkar
Head of DCTx Incubator Operations, UCB
LinkedIn Profile
Ouriel Barzilay
CTO, DermaDetect
LinkedIn Profile
Dr. Christina Biermann
Head Application Development & Integration, Bayer Pharmaceuticals
LinkedIn Profile
Spencer Jones
Digital Health Lead Global Drug Development, Oncology, BMS
LinkedIn Profile
Jorge Juan Fernández García
Director of Innovation, EIT Health
LinkedIn Profile
Jennifer McCormack
Connected Health Skillnet Manager, IBEC
LinkedIn Profile

Masterclass: Future EU Regulations for AI in Medical Devices

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.

When:
13th December @ 10AM GMT / 6PM AWST
Apply to attend
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