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Reg Talk Medical Engineering: Implementing IMDRF Codes - A Guide for Companies

Date & Time

from
03/06/202513:55 pm
until
03/06/202515:15 pm
duration
1hour

Location

place
MS Teams
city
Offenbach am Main Deutschland

Contact

Last name
Ms. Helena Däsch
VDE Verband der Elektrotechnik Elektronik Informationstechnik e.V.
phone
0698306876
email

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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