EMA — authorised 15 November 2021
- Marketing authorisation holder: BIOGEN NETHERLANDS B.V.
- Status: approved
EMA authorised Vumerity on 15 November 2021
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. EMA authorised it on 15 November 2021.
BIOGEN NETHERLANDS B.V. holds the EU marketing authorisation.