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1ISG-010 The cost of lacking regulatory clarity for nanosimilars

BACKGROUND: Today up to 23 nanomedicines are approved, and approximately 50 are in clinical development. In the past, first follow-on products also referred to as nanosimilars have entered the European market through the generic approval pathway. Significant differences have been observed in clinica...

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Bibliografische gegevens
Gepubliceerd in:Eur J Hosp Pharm
Hoofdauteurs: Flühmann, B, Mühlebach, S
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BMJ Group 2018
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7535185/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/ejhpharm-2018-eahpconf.10
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