There are significant changes in the European legislation applicable to IVDs. The IVD Regulation (EU 2017/746) has replaced the IVD Directive (98/79/EC), and will impose new requirements on manufacturers and other Economic Operators.

This long awaited text brings a number of significant changes to the regulatory requirements for IVD manufacturers, addressing the challenges posed by the IVD Directive. The changes include a new rule-based classification system, increased scrutiny of technical documentation, and improved traceability of devices through the supply chain.

Our one day training course has been designed to introduce IVD manufacturers and other Economic Operators in the supply chain to the key changes to requirements for CE marking following the publication of the new IVD Regulation (IVDR).  

Online training courses: Connected Learning Live
You can attend this training course classroom based and online. Do you prefer the convenience of an online training course? View here for the available dates or read more about Connected Learning Live.

Combination discount

Attending several medical device courses is associated with special combination discount.

1. Transition or Requirements IVD - IVDR
2. Implementing CE Marking IVDR
Combination training 1 + 2 

In-house training courses
For more information about combination of courses or in-house training courses, please contact our Training Advisors via +31 20 346 0780 or send an email to

For further information regarding reduced rates at the hotel where the training is being conducted please contact us.