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Pharmaceutical Engineering Unveiled: The Art and Science of Drug Manufacturing

, , , 978-93-6252-473-7 PAPERBACK FIRST EDITION , ,

The field of pharmaceutical engineering stands at the confluence of science and
technology, playing a pivotal role in the development, production, and
regulation of pharmaceuticals. “Pharmaceutical Engineering Unveiled: The Art
and Science of Drug Manufacturing” aims to provide an in-depth exploration of
this dynamic and essential discipline, offering a comprehensive guide for
students, educators, and professionals.
The motivation behind this book is rooted in the growing need for a detailed,
yet accessible, resource that bridges the gap between theoretical principles and
practical applications in pharmaceutical engineering. With the rapid
advancements in drug manufacturing technologies and the ever-evolving
regulatory landscape, it is crucial for current and future professionals to be
equipped with the knowledge and skills necessary to navigate these
complexities effectively.
This book is structured to cover the fundamental concepts of pharmaceutical
engineering, including drug development processes, manufacturing techniques,
quality control, and regulatory compliance. Each chapter is meticulously crafted
to provide both theoretical insights and practical guidance, ensuring that readers
gain a holistic understanding of the subject matter.
The first section of the book delves into the basics of pharmaceutical
engineering, outlining the principles of drug discovery and development. It
provides a solid foundation in the chemical, biological, and engineering aspects
that underpin the creation of pharmaceutical products.
The subsequent sections focus on the various manufacturing techniques and
technologies employed in the industry. From traditional methods to cuttingedge innovations, these chapters offer detailed explanations and real-world
examples to illustrate the practical applications of these techniques.
Quality control and regulatory compliance are also extensively covered,
highlighting the critical importance of maintaining high standards throughout
the drug manufacturing process. Readers will gain insights into the stringent
regulations governing the industry and the best practices for ensuring
compliance and quality assurance.

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