Medical device combination products: what regulations should you apply before marketing them in the EU?

• Questions & Answers for applicants, marketing authorization 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) (europa.eu)
• MDR Article 117: A New Implication for Drug-device Combination Products (celegence.com)

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