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Analysis of the Regulatory Requirements for Biosimilars in the EU

Analysis of the Regulatory Requirements for Biosimilars in the EU

A General Overview

AV Akademikerverlag ( 14.06.2016 )

€ 26,90

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A biosimilar is a biological medicinal product which is a copy of an original (innovator) product. The innovator product is often manufactured by a different company and after the patent of the innovator product expires a biosimilar can be registered in the European Union to a lower price than the innovator product. The first biosimilar in the European Union was registered in 2006 and was a Somatropin compound. Now are about 20 biosimilars registered in the European Union. Forecasts expect that there will be a huge amount of biosimilars pushing on the market in the near future and that will have a big influence on the industry.

Buch Details:

ISBN-13:

978-3-639-88881-2

ISBN-10:

3639888812

EAN:

9783639888812

Buchsprache:

English

von (Autor):

Kerstin Zörweg

Seitenanzahl:

68

Veröffentlicht am:

14.06.2016

Kategorie:

Pharmazie