FLYER | Regulation (EU) 2017/745: Understanding its impact on Drug-Device Combinations in Directive 2001/83/EC

Drug–device combination products (DDCs) and how are they classified in Europe

Drug–device combination products (DDCs) and how are they classified in Europe

DDCs incorporate a medical device component and a medicinal product component, under EU frameworks: Regulation (EU) 2017/745 (MDR) and Directive 2001/83/EC (MPD).

On this flyer, we show you what integral DDSs are and how they are classified in Europe.

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May 6, 2025
| By Asphalion

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