Medical Devices Update: discover fresh insights from the latest study on the implementation of Article 17 of Regulation (EU) 2017/745 concerning medical devices in the EU market.
This article governs the reprocessing of single-use devices in the EU market, assessing its implementation across 30 European countries.
Key Findings: Unveil challenges and opportunities, from certification processes to sustainability benefits.
Actionable Recommendations: Equip stakeholders with steps to enhance Article 17 implementation.
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Read the Full Report here: https://lnkd.in/dBisP4Hp
Know more about how to implement the Art. 17 of MDR into your health institution at: https://lnkd.in/dt4tQYNy