Webinar: Navigating AI Act Compliance in Medical Devices

We hosted our webinar, Navigating AI Act Compliance in Medical Devices, on Tuesday 9 September at 4.00pm - 5.00pm (Irish Time), via Zoom.

This year, we turned our attention to the practicalities of implementing the AI Act. We explored what the new regulatory landscape means in real terms for medical device manufacturers

We covered:

• Insightful discussion with legal, industry and notified body experts
• Key implementation steps and compliance timelines
• What manufacturers should prioritise now to remain competitive and compliant
  

Speakers included legal advisors from Mason Hayes & Curran, alongside representatives from industry and notified body TÜV SÜD.

Panellists:

• Brian McElligott, Partner & Head of Artificial Intelligence (AI) Mason Hayes & Curran
• Jamie Gallagher, Partner, Life Sciences Regulatory, Mason Hayes & Curran
• Marco Caproni, Global Director Software Product Assessment, TÜV SÜD
• Dr Shweta Agarwal, Director and Principal Regulatory Consultant, Cqura Ltd

This event was chaired by Michaela Herron, Partner and Head of Life Sciences, Mason Hayes & Curran.

60 Minute Watch | 1 CPD Point

Instructions

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• When finished watching click the link and fill out your *details
• A CPD certificate will be in your inbox within minutes

For any queries, please contact our events team at events@mhc.ie

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