Q&A on practical aspects related to the implementation of the extended transitional period provided for in the IVDR, as amended by Regulation (EU) 2024/1860

Name: Q&A on practical aspects related to the implementation of the extended transitional period provided for in the IVDR, as amended by Regulation (EU) 2024/1860
Creator: European Commission
License: https://creativecommons.org/licenses/by/4.0/
Keywords: eu,european-union,guidances,implementation,in-vitro-diagnostics-regulation,ivdr,q-a,questions-and-answers,regulations

Information

Type

Guidance

Regulated products

IVDMD, Medical Devices

Topics

Published

July 9, 2024

Last updated

July 9, 2024

Description

Document covers Q&A on practical aspects of implementing extended transitional period in the IVDR, as amended by Regulation (EU) 2024/1860.

Organization

European Commission 🇪🇺

Country / Region

European Union

License

Creative Commons Attribution 4.0

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1 Main file

Q&A

Updated on July 9, 2024

pdf

URL: https://health.ec.europa.eu/document/download/dfd7a1c6-f319-4682-9bac-77bef1165818_en?filename=mdr_qna-ext-ivdr.pdf
Permalink: https://data.openrid.co/en/datasets/r/8f232aff-efca-4324-826f-1ce927f2f58e
MIME Type: application/pdf

Created on: July 9, 2024
Modified on: July 9, 2024