In Vitro Diagnostic Regulations EU 2017/746 - What are they?
Understanding the IN VITRO DIAGNOSTIC REGULATION (IVDR) Everything You Need to Know
In Vitro Diagnostic Device Regulation (IVDR)
The IVD Directive and borderline products
Overview of EU regulations for in-vitro Diagnostic Medical Devices
EU Regulation Medical Device | IVDD | Directive 98/79 EC | What is EU MDR 2017 | IVDR | Lecture-2
Upcoming revisions of EU regulations & the reclassification of In Vitro Diagnostics
EU Regulation|Directive 98/79/EC of the European Parliament and Council|In-Vitro Medical Device|L-1
IVDR tutorial for diagnostic labs 1: Definitions, urgency, transition IVDD to IVDR
Medical Device & IVD regulations, impacts for MD manufacturers
BD: By your side through IVDR - Episode 7
Overview of the In-Vitro Diagnostic Medical Device Regulatory Landscape
What Are The New EU IVDR Regulations & How Are They Different To IVDD?
IVD Technical File Compilation
IVDR Checklist for Obtaining CE Marking & Maintaining EU Market Access
Evolutions in the EU IVD Regulatory Framework
Navigating the In Vitro Diagnostic Regulation (IVDR) Rollout for Legacy & New Devices - Webinar
All Hands on Deck! Transition Successfully to the New EU IVD Regulations 1
Tea Time Talks with MDRP- EU In Vitro Diagnostic Regulation (IVDR)
EU medical device and diagnostic regulatory overhaul: The Regulatory implications