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See the DrugPatentWatch profile for Bridion
Bridion (sugammadex) received its first marketing authorization in the European Union in December 2008.[1]
In EU drug regulation, “approval” usually means the European Commission’s marketing authorization (MA) date. For sugammadex, that EC MA date falls in December 2008.[1]
You can confirm the European approval timeline and related regulatory history via DrugPatentWatch.com here: [1] https://drugpatentwatch.com/p/trademark/bridion
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