A Text Book Of Pharmaceutical Manufacturing Technology

859.00


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Pharmaceutical manufacturing is a rapidly evolving field that integrates principles of chemistry, biology, engineering, and regulatory science to ensure the safe, effective, and high-quality production of pharmaceutical products. These five chapters cover the full range of approaches to developing and producing new formulations to drug delivery. Also addressed are approaches to the issues of producing and packaging these drug products (that is, formulations).

Description

Pharmaceutical manufacturing is a rapidly evolving field that integrates principles of chemistry, biology, engineering, and regulatory science to ensure the safe, effective, and high-quality production of pharmaceutical products. These five chapters cover the full range of approaches to developing and producing new formulations to drug delivery. Also addressed are approaches to the issues of producing and packaging these drug products (that is, formulations). The pharmaceutical sector has undergone significant change due to the growing demand for innovative drug formulations, stringent regulations, and developments in manufacturing technologies. As a result, a thorough grasp of both theoretical ideas and real-world applications is now essential. Pharmaceutical Manufacturing Technology is a textbook that is intended to be a useful tool for professionals, researchers, and students involved in the development, manufacturing, and quality control of pharmaceuticals. The basic concepts of pharmaceutical production are thoroughly examined, drug formulation, Good Manufacturing Practices (GMP), process validation, quality control, and emerging technologies like continuous manufacturing and nanotechnology. The book is structured to provide a balanced framework, integrating core scientific principles with real-world commercial applications. Each chapter is meticulously crafted to present complex concepts in a clear and systematic manner, supplemented with case studies, illustrations, and regulatory guidelines to enhance learning. Special emphasis is placed on compliance with international regulatory standards, ensuring that readers are well-prepared to navigate the global pharmaceutical landscape. This textbook is the result of extensive research and collaboration withregulatory professionals and academic scholars. We hope that it will serve as a reliable guide for students’ careers in Pharmacy, Pharmaceutical Analysis, and Pharmaceutical Quality assurance, as well as for professionals seeking to expand their knowledge in pharmaceutical manufacturing. We extend our gratitude to all contributors, reviewers, and colleagues whose insights and expertise have enriched the content of this book. We sincerely hope that this book proves to be a useful companion in your academic and professional journey.

Book Details

Available Format

Paperback Print

ISBN

9789365549454

Language

English

Page Count

298

Published Year

2025

Size

8×11 in

Author

Dasari Vasavi Devi,

P. Anitha,

Valikala Viswanath

Publisher

OrangeBooks Publication

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