12 Jun - 13 Jun 2025
MedTech Summit 2025
About Event
ACCESS MEDICAL DEVICE AND IVD MARKETS AT THE FLAGSHIP REGULATORY EVENT OF THE YEAR
Save Time, Effort, and Money While Ensuring Compliance with Global Regulations, and Engaging with the EU Commission, Notified Bodies, Competent Authorities, Working Groups, and Manufacturers
Gain Comprehensive Insights for Medical Device and IVD Manufacturing. 8 Vital Topics: EU MDR, IVDR, Clinical Evaluations & Investigations, Performance Evaluations, Post-Market Surveillance, Software & AI/ ML, Biocompatibility, Law & Compliance, and Global Market Access.
UK Participating companies - A-Z
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