Date & Time
- from
- 29/05/202412:00 pm
- until
- 29/05/202414:00 pm
- duration
- 2hours
The IMDRF codes, also known as "Terminologies for Categorized Adverse Event Reporting" provide a standardised method for describing and classifying incidents related to medical devices. Developed at a global level, the IMDRF codes are already widely used in post-market surveillance at EU level.
In this course, you will learn how to recognise and navigate the code structure. Several examples will be used to teach you how to use the IMDRF codes in a practical way. The event also offers plenty of time for your questions.
Further informationThe above texts, or parts thereof, were automatically translated from the original language text using a translation system (DeepL API).
Despite careful machine processing, translation errors cannot be ruled out.