How can we help you?

What assistance does Climedo offer with regard to the EU MDR (Medical Device Regulation)?

Together with our external consulting partners, we offer one-day and multi-day workshops on topics such as EU MDR, incentivizing product users, PMS and PMCF, etc. Our target groups are Regulatory Affairs and Clinical Affairs managers of manufacturers as well as product users and Key Opinion Leaders (KOL).

You can find free downloads about the EU MDR here.