Webinar Features
Impact of the EU AI Act on Medical Device and IVD Manufacturers
This webinar covers the regulatory changes and compliance requirements of the AI Act for manufacturers and stakeholders in the medical sector.
Format
On-Demand Webinar
Level
Basic
Trainer
Coenraad Davidsdochter
Certificate
Certificate of Participation included
Duration
45 minutes
Price
Free
Comprehensive Regulatory Expertise
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Flexible Viewing
Gain insights from industry experts and stay updated on the latest trends and regulations without the need to attend live sessions.
Access to Expertise
Meet the Trainer
Coenraad Davidsdochter
Coenraad Davidsdochter, a Senior Consultant in Software and Artificial Intelligence, brings over 20 years of software development experience and more than a decade in establishing and managing Quality Management Systems (QMS) compliant with ISO 13485, MDD 93/42/EEC, MDR 2017/745, and GDPR 2016/679, and has extensive expertise in areas such as technical file documentation, risk management, clinical evaluations, and information security.
