How should you manage the IVDR transition period for your device? [IVDR 2017/746]
![How should you manage the IVDR transition period for your device? [IVDR 2017/746]](https://img.youtube.com/vi/18tegmDCj3Y/0.jpg)
How will the IVDR Impact You?Подробнее
Preparation for the In Vitro Diagnostic Regulation IVDR 2017/746Подробнее
#IVDRonair video series: new IVDR transition timelinesПодробнее
Unique Device Identification (UDI)Подробнее
IVDR tutorial for diagnostic labs 2: IVDR structure, transition timelineПодробнее
Your Journey to IVDR Certification – A Roadmap to 2022Подробнее
On-Demand Comprehensive EU-IVDR 2017/746 Practitioner Training [Explainer Video]Подробнее
![On-Demand Comprehensive EU-IVDR 2017/746 Practitioner Training [Explainer Video]](https://img.youtube.com/vi/nwtAKUuZVa0/0.jpg)
How to regulate Self Testing with the new IVDR 2017/746?Подробнее
How to write your Performance Evaluation [IVDR 2017/746]Подробнее
![How to write your Performance Evaluation [IVDR 2017/746]](https://img.youtube.com/vi/xponsfV2OVA/0.jpg)
Managing the Tranisition to the IVDRПодробнее
Overview of the new EU- In-vitro Diagnostics regulation.Подробнее
Understanding the IN VITRO DIAGNOSTIC REGULATION (IVDR) Everything You Need to KnowПодробнее
FAQ Medical Device Economic Operators ? (EU MDR and IVDR)Подробнее
Changing Requirements for Manufacturers Under IVDRПодробнее
Is it the end of In-house devices? [IVDR 2017/746]Подробнее
![Is it the end of In-house devices? [IVDR 2017/746]](https://img.youtube.com/vi/AbwaA7DpbYI/0.jpg)
In Vitro Diagnostic Regulations EU 2017/746 - What are they?Подробнее
What are the new rules for In-Vitro Diagnostic Industry with IVDR 2017/746?Подробнее
IVDR Checklist for Obtaining CE Marking & Maintaining EU Market AccessПодробнее
Smart technology enables a holistic, data-driven approach to EU MDR/IVDRПодробнее
MDR & IVDR transition + Expert Panel Handover to EMA with Erik VollebregtПодробнее
MDR & IVDRПодробнее
