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Biosimilars (ne)jen v onkologii – dnešní realita i budoucnost
Authors: R. Demlová 1,2
Authors‘ workplace: Oddělení klinických hodnocení, Masarykův onkologický ústav, Brno 1; Farmakologický ústav LF MU, Brno 2
Published in: Klin Onkol 2014; 27(1): 64-66
Category: Oncology Highlights
Overview
Submitted:
12. 12. 2013
Sources
1. Kresse GB. Biosimilars – science, status, and strategic perspective. Eur J Pharm Biopharm 2009; 72(3): 479–486. doi: 10.1016/j.ejpb.2009.02.014.
2. Egagenerics.com [homepage on the internet]. European Genetic Medicines Association. c2004–2012 EGA. Available from: www.egagenerics.com.
3. Ema.europa.eu [homepage on the internet]. European Medicines Agency. United Kingdom c1995–2014 EMA. Available from: www.ema.europa.eu.
4. Krämer I. Pharmacy and pharmacology of biosimilars. J Endocrinol Invest 2008, 31(5): 479–488.
5. Zuñiga L, Calvo B. Biosimilars approval process. Regul Toxicol Pharmacol 2010; 56(3): 374–377.
Labels
Paediatric clinical oncology Surgery Clinical oncology
Article was published inClinical Oncology
2014 Issue 1-
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