The EU Artificial Intelligence (AI) Act implementation for Medical Devices SPIN webinar will provide a comprehensive overview of the impact of the EU AI Act on medical devices. It will highlight key milestones and offer practical recommendations to help manufacturers ensure compliance.
This session is free for TOPRA members to attend and is aimed at regulatory affairs professionals who are keen to stay ahead in the evolving field of Software as a Medical Device (SaMD) and AI as a Medical Device (AIaMD).
It is hosted by our SaMD and digital health Special Interest (SPIN) group, one of our many SPIN communities that provides a forum for discussion and networking for regulatory affairs professionals working in the same specialist sector.
Non-members are welcome to attend at a cost of £45, which also includes 2 months of free TOPRA membership.
