Webinar Features
Navigating Companion Diagnostics Under IVDR: Key Considerations for Standalone IVD Performance Studies
Stay ahead of the latest EU MDR developments with practical insights that help you navigate regulatory changes with confidence.
Format
On-Demand Webinar
Level
Beginner
Trainer
Daphne Smit-van den Hof
Exam
Certificate of Participation included
Duration
1 hour
Price
Free
Comprehensive Regulatory Expertise
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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
Daphne Smit-van den Hof
Daphne is a seasoned Senior Clinical Project Manager based in The Netherlands, bringing 18 years of clinical trial experience across hospitals and CRO environments, known for her practical leadership in full service project management, her strong background in interventional studies across multiple pathology areas, and her clear, solution driven communication style that keeps complex Pharma, Medical Device, and IVD trials running smoothly and in full compliance.
