We held our What the AI Act means for Medical Devices webinar in May.
By watching our CPD on Demand you can avail of a CPD certificate at the end of the video. Note it is not possible to fast forward or rewind the content.
During this webinar, we consider the impact of the AI Act on the medical device industry. Through Q&A with experts from industry, legal and notified body TÜV SÜD, we consider what the AI Act means for medical device manufacturers, what changes will be coming into effect and what manufacturers should be doing now to prepare.
Our expert speakers discuss these issues through the lens of legal, regulatory and notified body requirements, specifically:
- The gap between current compliance for AI medical devices and when the AI Act applies
- What real world challenges manufacturers will face in addressing that gap
- How the new combined conformity assessment procedure will look, and
- What all of this means in practical terms with a focus on data and documentation requirements
Panellists:
- Brian McElligott, Partner & Head of Artificial Intelligence (AI) Mason Hayes & Curran
- Marco Caproni, Senior Product Specialist Software, TÜV SÜD
- Shweta Agarwal, Director and Senior Regulatory Consultant, Cqura Ltd
This event is chaired by Michaela Herron, Partner and Head of Life Sciences, Mason Hayes & Curran.
60 Minute Watch | 1 CPD Point
Instructions
- Enter your email address in the video to begin the session
- 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
*When you submit your details, you will be added to the MHC Brief. We regularly produce insights on key legal issues in the Irish market. View our Privacy Policy Here
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