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▶ 주제: In-house tests under EU IVDR - How to best meet your IVDR deadlines
▶ 일시: 2024년 02월 28일 CST 9시 (한국시간: 02월 29일 자정)
The In Vitro Diagnostic Medical Devices Regulation (IVDR) (EU) 2017/746 is not only affecting legal manufacturers (companies) but also clinical laboratories using in-house tests. Though not all requirements apply to clinical laboratories, they must maintain technical documentation and update their quality management system to comply with the IVDR and national laws. The amended and phased implementation of the IVDR has set the first deadline to some of these requirements for May 2024.
This webinar will help you get a deeper understanding of the new IVDR requirements for clinical laboratories or parties involved in the manufacture or use of in-house tests. The presenter will explain the required actions in the remaining time (sprint) and share practical examples of how to comply with the IVDR in the long term (marathon).
In-house Tests Under EU IVDR – How to Best Meet Your IVDR Deadlines | Emergo by UL
In-house Tests Under EU IVDR – How to Best Meet Your IVDR Deadlines
In this complimentary webinar, our Emergo by UL subject matter expert will navigate through current regulatory requirements under IVDR.
www.emergobyul.com
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