The New European legislation on medical device regulation, the MDR, has been moving the market. That is because manufacturers of medical equipment need to adapt quickly to new requirements.
The Tubantia has written an article about how the MDR is already being followed in the production of the new mammogram apparatus. In addition, the publication has spoken with Lisette van Steinvoren, responsible for Medical Devices Development at Holland Innovative, about how her work has been assisting producers of medical equipment in product and process development. Read the full article here.
This week, Van Steinvoren was also at the TechMed Event 2019 talking about MDR, while conducting the lecture “Hear the Patient’s Perspective: A Key Element in Medical Device Development According to the MDR, but how to arrange it?“.