Do you work with Medtech, and you need to learn more about MDR?

Swedish Medtech, together with the Swedish Medical Products Agency, is offering a free webinar tailored for Class 1 manufacturers about the Medical Device Regulation (MDR). 

Part 2 of the webinar will be held on February 24th and will focus on Go-to-Market and Post-Market Surveillance.  

If you missed Part 1 of the webinar covering Pre-Market activities, a recording of the session is available for FREE. 

Don’t miss out on this opportunity to learn more about the regulatory requirements overseeing the medical device product lifecycle.

Learn more

Do you need support with your clinical investigations?

At Scandinavian CRO, we have the medical device expertise to help you with all aspects of your clinical investigations from planning, designing, and executing through to analysis and reporting. Contact us


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