🇪🇺 Hemlibra in European Union

EMA authorised Hemlibra on 23 February 2018

Marketing authorisation

EMA — authorised 23 February 2018

  • Marketing authorisation holder: Roche Registration Limited
  • Status: approved

Hemlibra in other countries

Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.

Other Hematology approved in European Union

Frequently asked questions

Is Hemlibra approved in European Union?

Yes. EMA authorised it on 23 February 2018.

Who is the marketing authorisation holder for Hemlibra in European Union?

Roche Registration Limited holds the EU marketing authorisation.