EU Medical Device Regulation (MDR 2017/745) and UKCA Mark Introduction
Please be invited to attend the webinar on the topic “EU Medical Device Regulation (MDR 2017/745) and UKCA Mark Introduction” for exporting medical devices to the EU and UK markets.
May 25, 2022, 14:00
May 25, 2022, 15:00
This webinar will introduce EU Medical Device Regulation (MDR 2017/745) and UKCA Mark. The speaker will present the most important regulation, including trends in the medical device market and who is the Key players and Economic Operators. These apply to all manufacturers and distributors that want to sell medical devices in the EU & UK. The engrossing contents are as follows.
1. What is CE marking
2. What is Medical Device Regulation
3. Key Players including Economic Operators
4. Approach for CE Marking (Steps for CE marking)
4.1. Definition of medical device
4.2. Classification of medical devices
4.3. Conformity assessment procedures
4.4. General Safety and Performance Requirements
4.5. Technical Documentation
5. UKCA – What you need to know?
6. CE marking in the UK after Brexit
7. Placing device on the UK market
This webinar is suitable for medical device business and related fields who are interested to export or trad the medical device’s product to the EU & UK.
Cost: No charge