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Questions & Answers for applicants, marketing authorisation holders of medicinal products and notified bodies with respect to the implementation of the Medical Devices and In Vitro Diagnostic Medical Devices Regulations ((EU) 2017/745 and (EU) 2017/746) EMA/321925/2021 Rev.2 Page 4/13 1. Combinations of medicinal products and medical devices 1.1.

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