Drug Regulatory Affairs

By:

Gajendra Singh ,Gaurav Agarwal and Vipul Gupta

Material type: Text

TextPublication details: CBS Publishers & Distributors 2015Edition: 1ISBN:

9788123928814

Subject(s):

Drug discovery and Development

DDC classification:

615 GAJ-D

Summary: The book is written with the main objective to explain the fundamentals of drug regulation to the reader in the simplest possible language and easy to understand manner. It keeps the balance between the basic essentials and advanced areas of knowledge, apart from the usual topics. The effort has been mainly to focus on the primary aspects for students of postgraduate courses in pharmacy and people working in DRA department of pharmaceutical industry. It seems to be one of the finest efforts of its own kind to offer a wide range of various fundamentals in this field from the very traditional to the modern trends of regulatory affairs in pharmaceuticals. The text deals not only with the basic concepts but also emphasizes the technical and practical aspects of the subject. This book will help in bridging the existing gap of knowledge among budding pharmacy technocrats, academicians and scientists, especially the young professionals of drug regulatory department in pharmaceutical industry

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Holdings
Item type	Current library	Home library	Call number	Status	Date due	Barcode
Book	Dept. of Computational Biology and Bioinformatics Processing Center	Dept. of Computational Biology and Bioinformatics	615 GAJ-D (Browse shelf(Opens below))	Available		DCB2923

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The book is written with the main objective to explain the fundamentals of drug regulation to the reader in the simplest possible language and easy to understand manner. It keeps the balance between the basic essentials and advanced areas of knowledge, apart from the usual topics. The effort has been mainly to focus on the primary aspects for students of postgraduate courses in pharmacy and people working in DRA department of pharmaceutical industry. It seems to be one of the finest efforts of its own kind to offer a wide range of various fundamentals in this field from the very traditional to the modern trends of regulatory affairs in pharmaceuticals. The text deals not only with the basic concepts but also emphasizes the technical and practical aspects of the subject. This book will help in bridging the existing gap of knowledge among budding pharmacy technocrats, academicians and scientists, especially the young professionals of drug regulatory department in pharmaceutical industry

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