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New EMA guidelines on biosimilar medicines

1 June 2017 | By Niamh Marriott, Junior Editor

The European Medicines Agency (EMA) and the European Commission have published an information guide for healthcare professionals on biosimilar medicines...

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Sandoz proposed biosimilars recommended for EU approval

25 April 2017 | By Niamh Marriott, Junior Editor

The Committee for Medicinal Products for Human Use (CHMP) has adopted positive opinions, separately recommending the approval of both Sandoz's (a Novartis division) biosimilar rituximab and biosimilar etanercept in Europe, to treat the same indications as their respective reference medicines.