1ISG-020 Market access in the eu, do we have enough evidence?

BACKGROUND: The European Medicines Agency (EMA) is responsible for the scientific evaluation of medicines for use in the European Union (EU), providing a scientific opinion on the granting of EU-wide marketing authorisations. PURPOSE: We conducted a retrospective analysis of new active substances (N...

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Detaylı Bibliyografya
Yayımlandı:Eur J Hosp Pharm
Asıl Yazarlar: Lluch, T Gómez, Fuentes, MD Fraga, Aroyo, P Araque, Dongil, C Notario, Gámez, JC Valenzuela, Benito, M Heredia
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BMJ Group 2018
Konular:
Section 1: Introductory statements and governance
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7535274/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/ejhpharm-2018-eahpconf.20
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