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8 May 2025 | 09:00 and 16:00 BST
From a Notified Body standpoint, this webinar will provide guidance around the essential aspects of the AI Act and Medical Device Regulation.
Gain insights into the role of AI in Medical Device Regulation and the AI Act.
Understand assessment processes for AI-based medical software during and post-transition.
Learn how to prepare comprehensive technical documentation for MDR AI evaluations.
Recommended for start-ups, SMEs, developers, and medical device software companies.
Global Head, Active Implantable Medical Devices and SaMD
AI Regulatory Lead
Reach out and see how we can help guide you on your path to sustainable operational success.