From Classification to Post-Market Surveillance: A Comprehensive Comparison of FDA and EU IVDR Requirements for In Vitro Diagnostic Devices

Name: From Classification to Post-Market Surveillance: A Comprehensive Comparison of FDA and EU IVDR Requirements for In Vitro Diagnostic Devices
Start: 2026-11-18T16:20
End: 2026-11-18T16:35
Location: Messe Düsseldorf Fairground

MEDICA 2026 · 18 November 2026 · 16:20–16:35 · Hall 8a, G40

From Classification to Post-Market Surveillance: A Comprehensive Comparison of FDA and EU IVDR Requirements for In Vitro Diagnostic Devices was a session at MEDICA 2026 on 18 November 2026 in Düsseldorf, with 3 speakers on record.

Speakers

Jun Peng — Speaker P&L Scientific Inc.
Jens Ebnet — Chair
Susette Germer — Chair Founder & CEO, SalesPro4U - Top Expert Recruiting Agency