Training

In Vitro Diagnostic Regulation (EU) 2017/746

Training Methods: Virtual Training ○ On-Site ○ Bespoke

Course Overview

The EU IVDR will replace the current EU Directive on In Vitro Diagnostic Medical Devices (98/79/EC) and will be effective in all EU member states and EFTA states.

Our industry leading experts have created this 2-day IVDR course to give you an appreciation for the changes and understanding of the new requirements.

 

This IVDR training course provides practical skills and guidance on how to transition to the new regulation.

At A Glance

- 2-days of fully interactive training

- Instructor-led virtual classroom

- PDF Certificate of completion

- Live Q&A sessions

- PDF Copies of the slides, handouts and templates

- Full tutor support 

- Bespoke and on-site training available 

Who Should Attend?

This training course is recommended for anyone making and selling In vitro diagnostic devices into the European Union:

- Regulatory Affairs Professionals

- Research and Design Engineers

- Quality Managers

- Quality Engineers

- Authorised Representatives

- Consultants

"I really enjoyed the course, so many things finally clicked into place for me and I now feel much more confident in writing CER's. Worth every penny. Thank you so much!." 

Claire S

ConvaTec Group

MDR Training Reviews

"I can't fault this CER course, the delivery was excellent, as was the content and especially the trainer Rod. He clearly knows his stuff and that's what makes all the difference. This virtual training was the best I've ever done and I could find no fault. I'd definitely recommend this course to colleagues."

Gwen L

ConvaTec Group

MDR Training Reviews
"Fantastic to have an instructor with subject knowledge that was able to relate to the experience of participants. Presented and delivered at a good pace to allow understanding and ample opportunity for specific questions." 

Alan B

Terumo BCT

MDR Training Reviews

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