There are lots of great ideas and products related to medical device software today. Many of them already are compliant to the Medical Devices Directive (MDD), others are in an earlier development state.
Since May 26th, 2021, the Medical Devices Regulation (MDR) is in force and latest May 26th, 2024, all medical device software has to be compliant to MDR. The struggle for many manufacturers is that with MDR, in addition to providing the appropriate documentation, the majority of the medical device software providers now must find a suitable notified body to be able to CE-mark the software.
Join us on the 16th of December at 10:00 AM CET for a 20-minute live webinar where we will present:
- How you can find out if your software is qualified as a medical device software according to the Medical Devices Regulation (MDR)
- A roadmap to make your medical device software MDR compliant
- An indication of the timeline for the MDR CE marking process
Date: 16 December
Time: 10:00 AM CET
Speaker: Stina Gustafsson, Senior consultant Quality Assurance