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Switzerland: Swissmedic Enhances Fast-Track and Temporary Authorization Processes for Human Medicine (w.e.f 15 Oct 2024)
Swissmedic, the Swiss regulatory authority for therapeutic products, has introduced updates to its guidance documents for the Fast-track...

ARQon
Nov 5, 20242 min read
Europe - Aug 2019
Albania: Amendments proposed to ‘Law on Medical Devices’ EU: New MDCG documents on Notified Bodies, the person responsible for regulatory...

ARQon
Aug 30, 20191 min read
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