Team PRRC are running a webinar on the EU AI act and its impact on the MDR/IVDR framework:
🚨 New Webinar Alert – Organized by TEAM-PRRC 🚨
Navigating the EU AI Act: Practical Compliance Implications for PRRCs
Artificial Intelligence is no longer a future topic for MedTech. It is now a regulated reality.
With the entry into force of the EU AI Act, many PRRCs and regulatory leaders are asking fundamental questions:
• Does the AI Act apply to our organisation and to the devices we manufacture?
• How does it interact with the MDR/IVDR framework?
• What are the implications for the responsibilities of the PRRC?
• And how should RA/QA professionals position themselves in this evolving landscape?
Before looking at specific AI tools or solutions, it is essential to understand the regulatory architecture and governance framework introduced by the AI Act.
TEAM-PRRC is therefore pleased to announce a new webinar designed to provide a clear, structured and neutral overview of the AI Act requirements and their practical implications for MedTech organisations.
🎙 Presented by Maarten ter Mors, CEO of Raiana
Agenda:
• Overview of the EU AI Act and its key requirements for MedTech
• Practical compliance implications for manufacturers and PRRCs
• Presentation of Raiana and how it can support regulatory and quality professionals
• Open discussion and exchange with participants
Our objective is simple: equip PRRCs and regulatory professionals with the clarity and regulatory foundation needed to approach AI-related topics with confidence and critical perspective.
📅 March 17th | 16:00–17:00 CET
🎟 Free and open to all
🔗 Register here: https://lnkd.in/dUSvmkMG
If you are a PRRC, RA/QA professional, or regulatory leader navigating the impact of AI on compliance, this session is for you.
