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Join this event to hear the latest regulatory insights and guidance on the process of placing an in vitro diagnostic device on the market.
QMS under IVDR, including MDSAP
IVD Regulatory Update
Client Journey to Certification: a real-world example and lessons learned from IVDR submissions
Navigating IVDR – technical content Common pitfalls and the journey to success
AI Update
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Reach out and see how we can help guide you on your path to sustainable operational success.