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20160128 EGA Regulatory and Scientific Affairs Conferenc

Labelling & Naming – EBG Perspective, DIA Berlin 2014

3 December 2014

Policy

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WHO BQ Proposal – EGA’s perspective, 59th INN Consultation, WHO, Geneva, 14 October 2014

14 October 2014

Policy

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GfK – Factors Supporting a Sustainable European Biosimilar Medicines Market

9 September 2014

Report

A study about the future sustainability of the biosimilar medicines […]

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EMA mAb Workshop – Guideline on Similar Biological Medicinal Products

31 October 2013

Policy, Video

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EMA mAb Workshop – Quality Target Product Profile in the Development of a Biosimilar

31 October 2013

Policy, Video

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EMA mAb Workshop – Stepwise Approach to Non-Clinical Program

31 October 2013

Policy, Video

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International Generic Pharmaceutical Alliance (IGPA) Letter Regarding TGA Guidance Titled “Evaluation of Biosimilars”, 2013

18 September 2013

Policy

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Safe Prescription,Safe Dispensing, Identification and Track&Trace of All Biologicals in the Context of the Re-opened Biosimilars INN Debate – 11th EGA Symposium on Biosimilar Medicines, Suzette Kox, London 2013

25 April 2013

Policy

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Biosimilar Monoclonal Antibodies – 11th EGA International Symposium on Biosimilar Medicines, Gudbjorg Edda Eggertsdottir, London, 25 April 2013

25 April 2013

Policy

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Production and Control of Biosimilars versus Innovators, Biosimilars Present and Future – Da Silva, Infarmed, Lisbon, 3 April 2013 (PPT)

3 April 2013

Policy

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