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- W2501926815 abstract "INTRODUCTION This chapter presents an overview of the current Good Manufacturing Practice (cGMP) regulations for parenteral drugs. Since most of the major world regulatory authorities follow either the U.S. or the European Union (EU) model for their GMP regulations, this chapter will focus only on these two regulations." @default.
- W2501926815 created "2016-08-23" @default.
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- W2501926815 date "2012-12-27" @default.
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- W2501926815 title "Development challenges and validation of fill and finish processes for biotherapeutics" @default.
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- W2501926815 doi "https://doi.org/10.3109/9781420086485-4" @default.
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