This book offers information on the fundamentals of the herbal drug industry, the quality of raw materials, and standards for the quality of herbal medications, herbal cosmetics, natural sweeteners, and nutraceuticals, among other things. The topic also places a strong emphasis on regulatory, patenting, and good manufacturing practices (GMP) concerns for herbal medicines. Herbal remedies have long been utilized extensively in both developed and poor nations. They are also very well-liked for their effectiveness, safety, and lack of negative side effects. However, the efficacy and safety evidence do not meet the standards required to enable their usage globally. To summarizes the fundamental knowledge of herbal drug technology, regulatory and patenting issues, as well as current herbal excipients, etc., we have written this book.
The title of the book is " PHARMACOGNOSY AND PHYTOCHEMISTRY I ". The writers' original intent for the book was to present a compiled database for PHARMACOGNOSY-I that was simple to understand. This book's purpose is to enlighten readers on cutting-edge drug delivery methods and to steer instructors and students toward key ideas in Pharmacognosy-I. The main goal of writing this textbook was to give material in a clear, concise manner to fulfill undergraduate students' needs in accordance with PCI guideline. This book was created to educate post-graduate students on pharmaceutical jurisprudence as well as adhere to the PCI curriculum for pharmacy undergraduate courses. We guarantee that graduates, postgraduates, lecturers, and industry learners will find this book to be of great use.
In the ever-evolving landscape of pharmaceutical sciences, the role of analytical techniques cannot be overstated. The quality, safety, and efficacy of pharmaceutical products hinge upon the precision and reliability of analytical methods employed throughout their development, manufacturing, and regulatory approval processes. The past few decades have witnessed remarkable strides in analytical instrumentation, methodologies, and data analysis, catalyzing a paradigm shift in pharmaceutical analytics. This book is conceived as a comprehensive guide to modern pharmaceutical analytical techniques, aiming to bridge the gap between theoretical knowledge and practical application in the dynamic pharmaceutical industry. It is designed to serve as an invaluable resource for students, researchers, and professionals engaged in pharmaceutical analysis, providing a systematic overview of the state-of-the-art analytical tools and strategies employed in drug discovery, development, and quality control. Each chapter is meticulously crafted to deliver comprehensive insights into the theoretical foundations, practical considerations, and recent advances pertinent to the respective analytical technique, supplemented with illustrative examples, case studies, and critical discussions. Moreover, special attention is devoted to emerging trends, such as nanotechnology-enabled analytical platforms, microfluidic-based assays, and in silico predictive modeling, underscoring the transformative potential of cutting-edge technologies in reshaping the landscape of pharmaceutical analytics. It is our fervent hope that this book will serve as a catalyst for fostering interdisciplinary collaboration, driving innovation, and advancing best practices in pharmaceutical analytical sciences. We extend our sincere gratitude to the contributors for their scholarly contributions and dedication, as well as to the readers for their interest and engagement in this endeavor.
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