EMA: Updated and revised Q&A on MDR and IVDR
21 October 2019 Rev.1
EMA/37991/2019
Human
Medicines Evaluation Division
Questions & Answers on Implementation of the Medical
Devices and In Vitro Diagnostic Medical Devices Regulations ((EU)
2017/745 and (EU) 2017/746)
This
Question and Answer (Q&A) document provides practical considerations
concerning the implementation of the medical devices and the in vitro
diagnostic medical devices regulations.
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