10 - 14 June 2024 + on-demand for 10 days | Digital Pass (Delivered in Central European Summer Time)
About: 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.
See agenda to learn more.