During the webinar, the speaker addressed the following topics:
- Regulation 2017/745 on medical devices applicable in the EU
- What are the differences between conformity assessment (registration) of medical devices in Ukraine and the EU?
- How to prepare the quality system and technical documentation for a medical device
- The EUDAMED database, post-marketing system, and other new requirements to implement before entering the market
The webinar provided valuable information for medical device manufacturers on entering the European market and the upcoming implementation of MDR 2017/745 in Ukraine.
Webinar recording available at this link, Vladislav’s presentation at this link.
On our website you can find the Training Events Plan for August 2024. We invite you to review it and participate in upcoming events.
Have questions? Email us at info@medquality.com.ua or call us, or contact us via your preferred messenger (Viber, Telegram, WhatsApp):
+38 095 557 37 37
