The European Medicines Agency (EMA) and the European Commission have published an information guide for healthcare professionals on biosimilar medicines.
Archive for Category: "Guidelines"
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A biobetter trastuzumab is on the way 
EGA president calls on Member States to boost market access for biosimilars in the EU 
3rd Forum on Biosimilars 
Pfizer starts biosimilar rituximab Phase I/II trial 
Indian Biosimilars Market 
World’s first biosimilar antibody* is approved in Korea 
A biosimilar manufacturer: Celltrion 
2 patents down, 1 to expire: Herceptin biosimilar coming to EU
January 12, 2017 8:26 AM
FDA announced the Guidance: ‘Clinical Pharmacology Data to Support a Demonstration of Biosimilarity to a Reference Product’
December 27, 2016 11:47 AM
Tailored scientific advice to support step-by-step development of new biosimilars in EU
