SAFETY AND CLINICAL EFFICACY IN BIOSIMILAR SUBSTITUTION

Biosimilar medicinal products have become a reality in recent years. Despite an established legal pathway for biosimilars in the European Union since 2005 and increasing regulatory guidance on data requirements for their development and approval, many clinicians are still reluctant to consider biosi...

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Hoofdauteurs: João Pedro Fernandes (Auteur), João Gonçalves (Auteur)
Formaat: Boek
Gepubliceerd in: Formifarma, LDA., 2015-03-01T00:00:00Z.
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3rd Floor Main Library

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