Do you have a bright idea and are stepping into the field of entrepreneurship and medical devices? Besides what a normal entrepreneur does, as finding customers, searching for money, making the first prototype, you will find additional challenges in the medical field. Like finalizing the MDR certification process. What does Medical Device Regulation mean in the MedTech segment? Which hurdles do you need to pass and how can we help you?
For entrepreneurs in Med Tech, those steps are doable, and we would like to explain you, during this Innovation Booster Podcast: how you can make small steps, to make a giant leap.
In this seventh episode of the Innovation Booster Podcast, we would like to make you aware of the MDR regulatory issues. And instead of viewing it as a pain in the ass hurdle, we aim to inspire you to turn this into a competitive advantage for your Business. We will dive into this very important topic with three experts in the field of Medical Device Regulation and the Medical Ethical Review Committee. First, we welcome Jelmer Sjollema, Assistant Professor in Biomedical Engineering at the UMCG and member of the METC). Secondly, we will welcome Ilona Brouwer. Ilona is a true expert in the development and implementation of medical devices and medical technology, and is are working as an Innovation Consultant at the UMCG Innovation Centre. Thirdly, we welcome Jan-Willem Veldsink, who is working as a Business Developer at the UMCG Innovation Centre.
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