Cargando...

Ten years of biosimilars in Europe: development and evolution of the regulatory pathways

A biosimilar is defined by the European Medicines Agency as a biological medicine that is similar to another biological medicine that has already been authorized for use. A science-based regulatory framework to ensure high-quality biosimilars has been established in Europe since 2005 and is monitore...

Descripción completa

Guardado en:
Detalles Bibliográficos
Publicado en:Drug Des Devel Ther
Autores principales: Schiestl, Martin, Zabransky, Markus, Sörgel, Fritz
Formato: Artigo
Lenguaje:Inglês
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC5440034/
https://ncbi.nlm.nih.gov/pubmed/28553082
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/DDDT.S130318
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!