Implementation of the Medical Device Regulation (MDR) for CE Marketing

Following the success on our first cohort taking place In early July 2019 we are happy to announce the 2nd course

This three days course aims to offer guidance on implementation of the requirements stipulated in the Medical Devices Regulation (MDR). It focusses on enabling you to draw up a clear concept or project plan, and how to integrate the requirements into your business and your documentation. Moreover, you should gain confidence and expertise to evaluate and implement more specific requirements on your own three-day training course

On completion, you will be awarded an internationally recognized BSI Training Academy Certificate 

About the course - click here

For the agenda – click here

For more information: idans@export.gov.il | 03-5142807  

For registration -  click here

25th-27th November

Metropolitan Hotel, 11 -15 Trumpeldor st. Tel-Aviv

Participation Fees:

IEI Members – 6,900 NIS | Non IEI Members – 12,000 INS 

Cancellation Policy:

Up to 14 days before the event