Internationalization of Drug manufacturing and the Quality of Pharmaceutical products

International Journal of Pharmacy and Biomedical Engineering

© 2016 by SSRG - IJPBE Journal

Volume 3 Issue 1

Year of Publication : 2016

Authors : Pidaparthi Praneeth

10.14445/23942576/IJPBE-V3I1P102

How to Cite?

Pidaparthi Praneeth, "Internationalization of Drug manufacturing and the Quality of Pharmaceutical products," SSRG International Journal of Pharmacy and Biomedical Engineering, vol. 3,  no. 1, pp. 3-5, 2016. Crossref, https://doi.org/10.14445/23942576/IJPBE-V3I1P102

Abstract:

The Internationalization of drug manufacture has increased day by day. As the production cost has increased, so the European countries and the rest of the world are shifting their manufacturing facilities to Asian countries like India, China etc. The Asian countries are playing a crucial role in drug manufacture (both API and Finished dosage forms). As the production increases, the quality of the product should also maintain the standards as per the regulatory requirements for human use. This article discusses the Internationalization of drug manufacture and challenges on the quality of pharmaceuticals.

Keywords:

Internationalization, API, Finished dosage forms.

References:

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