We are very happy to announce that the pilot episode of MDR-podden is here!
In this premiere episode “MDR 101” you’ll get a taste of what the podcast will address in the future. You’ll also get to know our Director of Regulatory Affairs Sofia Nordgren better as – for once – she’ll be answering the questions rather than asking them since Frida Lawenius from SwedenBIO is the guest host of the first episode.
The ambition of the podcast is to guide life science companies through the medical device regulations (MDR). In the upcoming episodes, MDR-podden will discuss and highlight what products will be affected by the new regulations; the transition period; CE-marking; classification; notified bodies; and the relationship between MDR and national laws and regulations.
Listen to the podcast on Spotify: