Celegence ([ Ссылка ]) provides the medical device industry with consulting services that are tailored to the evolving needs of manufacturers.
Our suite of services including EU MDR related support allows you to focus on your core responsibilities. With our guidance, bringing your devices to the market and keeping them there will be easier for your regulatory and quality teams.
Expanded Post Market Surveillance (PMS) requirements is a major hurdle that the EU MDR presents. Notified Bodies will be expecting a far greater amount of Post Market Surveillance data, and device manufacturers must improve their PMS systems and processes to adapt.
Why should you watch this webinar?
1. To better understand the MDR requirements for PMS
2. Learn about the purpose of PMS in the EU MDR
3. For an explanation of Article 83 and Article 84 of PMS
