Date & Time
- from
- 03/06/202513:55 pm
- until
- 03/06/202515:15 pm
- duration
- 1hour
Reg Talk Medical Engineering deals with the regulatory framework for medical devices. This time the focus is on IMDRF codes as an important aspect of post-market surveillance.
The IMDRF codes, also known as "Terminologies for Categorised 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 at EU level.
In this event, our expert Sophia Zoe Narten will show you how you can successfully implement the use of the IMDRF codes in your company. Benefit from her practical experience to overcome typical challenges and learn proven methods for implementation in your company.
We look forward to your participation!
For more information about the event, please see here.
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