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
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