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Written By Prof. V. Girija Sastry who is a distinguished Professor at A.U. College of College of Pharmaceutical Sciences with over three decades of academic and research experience.
This book offers an in-depth exploration of the essential principles and practices that define pharmaceutical process chemistry, bridging the gap between research and commercial production. Aimed at both students and professionals, it provides a comprehensive guide to the complexities involved in scaling up pharmaceutical production while ensuring that the processes are safe, efficient, and compliant with global standards.
Key Features:
In-Depth Coverage of pharmaceutical process chemistry, including reaction kinetics, extraction techniques, distillation, crystallization, and process optimization.
Detailed Exploration of green chemistry principles, highlighting the importance of sustainable practices in pharmaceutical manufacturing.
Comprehensive Overview of global regulatory frameworks such as FDA, EMA, ICH, and WHO, ensuring that pharmaceutical products meet safety, efficacy, and quality standards.
Practical Insights from case studies showcasing successful process optimization and scale-up strategies in the pharmaceutical industry.
This book is an indispensable resource for understanding the full spectrum of pharmaceutical process chemistry, from the development of active pharmaceutical ingredients (APIs) to the commercialization of pharmaceutical products.
