Impact of the MDR on the rules for reporting and notiing medical devices

On 26 January 2021, the "Impact of the MDR regulation on the rules for reporting and notiing medical devices" took place. The training was led by lawyers from the Life Science department of Kondrat and Partners Justyna Stefańczyk-Kaczmarzyk and Roksana Strubel. The webinar discussed the latest changes related to the electronic submission of notifications and notifications, the new registration obligations resulting from the MDR and the draft new law on medical devices, as well as the deadlines for the application of existing and new obligations.

We invite you to watch the recording of the training- https://youtu.be/Ft8X5Cmum0Y

Holler Box