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▶ 주제: Regulation (EU) 2024/1860 and IVDR Compliance in Europe
▶ 일시: 2024년 10월 16일 CST 9시 (한국시간: 10월 16일 23시)
Are you an IVD medical device manufacturer who needs a better understanding of what action you will need to take and when so that you can make use of the extension under the revised Regulation (EU) 2024/1860.
The European Commission amended the In Vitro Diagnostic Devices Regulation (EU) 2017/746 (IVDR), Article 110. This was done with the adoption of Regulation (EU) 2024/1860. The Regulation (EU) 2024/1860 introduces a staggered extension of the transition period provided for in the IVDR under certain conditions.
Join us as our own Heather Crawford explains what you need to know so that you can gain or maintain EU IVD market access.
Webinar: Regulation (EU) 2024/1860 and IVDR Compliance in Europe | Emergo by UL
Webinar: Regulation (EU) 2024/1860 and IVDR Compliance in Europe
In this complimentary webinar, our Emergo by UL subject matter expert will share insights on Regulation (EU) 2024/1860 and IVDR transition periods in Europe.
www.emergobyul.com
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