- Zoek in BSI
- Een certificaat verifiëren
Suggested region and language based on your location
Your current region and language
This one-day intensive course enables greater understanding of the key requirements for technical documentation for medical devices, in line with the European Medical Device Regulation (MDR) requirements in Europe. The aim of the course is to enable manufacturers to:
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.
Upon completion of this training, you will be able to:
QA/Regulatory personnel involved in compiling technical documentation; product design personnel and those in research and development for medical devices intended for the European market.
Prerequisites
You should have a basic understanding of European Medical Device Regulation (MDR).
Would you like to spend the night in the hotel before or during the training? We can reserve a hotel room for you at a reduced rate. If you would like to make use of this possibility, please contact us via training.nl@bsigroup.com.
In-house training courses
The training courses from the regular training offer can also take place at your location. These can be individual training sessions from the portfolio or a combination of training sessions. In most cases, the training courses can be given in both English and Dutch. Advantages of an in-house training:
Your employees:
For more information about in-house training, please contact Training on 020-346 0780 or send an email to training.nl@bsigroup.com.
Neem contact met ons op en ontdek hoe wij u kunnen helpen met het realiseren van duurzame groei en succes.