Minal Ghante - Böcker

This book, Green Analytical Chemistry in India: Innovations for a Sustainable Future, gives an overview of Green Analytical Chemistry (GAC), focusing on India's contributions, research advances, and uses in environmentally friendly analytical methods. It is meant to be a useful tool for students, researchers, and professionals who wish to use analytical methods that are good for the environment while still being efficient, reliable, and accurate.The book talks about important concepts of green chemistry that can be used in analytical science, like the E-factor, atom economy, and life cycle analysis, which help evaluate and reduce the environmental impact of analytical processes. It discusses the use of green analytical methods and the use eco-friendly solvents like ionic liquids, deep eutectic solvents, and water-based systems.A significant attention is paid to how GAC can be used in India, especially in areas like food safety, pharmaceutical analysis, environmental monitoring, industrial quality control, and forensic science. The book talks about how sustainable analytical methods can help laboratories and businesses follow the rules, cut down on chemical waste, and work more efficiently.The text also explores environmentally friendly chromatographic and spectroscopic methods, such as new developments in HPLC, GC, and green spectroscopic methods. It focuses on using less solvents, greener reagents, and instruments that use less energy. Discussion about emerging areas like green nanotechnology, biotechnology-based analytical tools, and using artificial intelligence to improve analytical methods. Supercritical fluid extraction, microwave-assisted extraction and solid-phase extraction are all examples of sustainable extraction methods that can be used instead of traditional ones.By integrating global principles of green analytical chemistry with India-specific innovations and case studies, the book highlights the growing importance of sustainable analytical methodologies in India’s academic, research, and industrial landscape.

The pharmaceutical quality system ensures that the process performance is suitably achieved, the product quality is regularly met, improved opportunities are identified and evaluated, and the knowledge is constantly expanded. Auditing also plays a crucial role within the pharmaceutical industry. It helps to assess and review quality to improve and build a better system for the benefit of companies.This book aims to develop a tool that will substantially decrease the number of Inspectional Observations and Warning letters, thus eliminating Import Alerts and Consent Decree. This book targets the Pharmaceutical Industry and students of Pharmaceutical Quality Assurance so they can get in hand-ready consolidated information on Pharmaceutical Quality guidelines, Quality metrics, and implementation of simplified SOP guidelines, plant layouts to implement Quality metrics for Pharmaceutical Manufacturing systems in tablets, capsules, liquid orals, and semi-solid dosage forms.The chapters cover the various aspects of Pharmaceutical Quality Assurance. The selection of topics is mainly based on the requirements of Pharmaceutical regulatory guidelines of India, the UK, the USA, Australia, and South Africa. Each chapter includes the abstract, detailed explanation, implementation guidelines, flowcharts, layouts, and Standard Operating Procedure of quality metrics for the Pharmaceutical Manufacturing System