About Book
The Textbook of Modern Pharmaceutics provides a comprehensive foundation in drug development, formulation science, and industrial pharmacy, It begins with essential preformulation concepts that explore physicochemical properties of drugs. A key focus is on drug–excipient interactions and various analytical methods used to study compatibility. The text explains stability kinetics and detailed stability testing procedures. It also covers theories of dispersion and the preparation of emulsions, suspensions, and SMEDDS. Stability considerations for large- and small-volume parenterals are thoroughly discussed. The book emphasizes physiological, formulation, and manufacturing aspects of parenteral products. Optimization techniques in formulation help scientists refine product quality and performance. Core optimization parameters are explained along with their role in pharmaceutical processing. Statistical designs, factorial models, and response surface methods are introduced for systematic experimentation. Contour plots and mathematical tools are highlighted for interpreting formulation outcomes. Validation concepts form a major section of the book, starting with an introduction to pharmaceutical validation. The scope, importance, and benefits of validation activities are clearly outlined. The book covers preparation and calibration of the master validation plan. ICH and WHO guidelines for equipment validation and calibration are included for global compliance. It further explains validation procedures for different dosage forms and manufacturing operations. Various types of validation, including prospective, concurrent, and retrospective, are described. Government regulations and manufacturing process models are also emphasized. The qualification steps URS, DQ, IQ, OQ, and PQ are detailed for facility validation. A separate section discusses cGMP principles and objectives for ensuring product quality. It includes GMP policies, building layout requirements, and essential utility services. Equipment selection, operation, and preventive maintenance practices are covered extensively. Industrial management topics focus on production systems, workforce organization, and materials handling. Inventory control, transportation methods, budgeting, and cost control strategies are also discussed. Total Quality Management concepts introduce continuous improvement and customer-focused manufacturing. The book concludes with advanced topics such as tablet compression physics, compaction behaviour, dissolution parameters, kinetic models, similarity factors, and statistical tools essential for product evaluation.
About Author
Prof. Navneet Verma is working as Pro Vice Chancellor of IFTM University, Moradabad. He obtained his B. Pharm degree from Uttar Pradesh Technical University, Lucknow, he did his M. Pharm from Bundelkhand University, Jhansi. Since last 20 years he is engaged in teaching of Pharmaceutics subject to the Undergraduate and Postgraduate students. Prof. Verma has received number of awards and recognitions from various societies. He has obtained his Ph.D. degree in Pharmaceutical Sciences in the year of 2013. Twenty-five M. Pharm dissertations and Ten Ph.D. degree has been awarded and Eight research scholars are enrolled for Ph.D. degree under his supervision. Prof. Verma is serving as reviewer board member of various National and International journals. He has, to his credit 78 research papers in International and National journals of high repute and 12 papers so far presented in various conferences, seminars and workshops. 19 patents are published by Prof. Verma in India as well as in other countries. He is an active member of various professional bodies in India. Currently, Prof. Verma is also holding the position of Dean, Faculty of Pharmacy, IFTM University, Moradabad.
Deepika Kumari is a dedicated pharmacy professional with a strong foundation in academics and research, currently pursuing a Ph.D. at Shri Venkateshwara University on atorvastatin-loaded transferosomal gel for hyperlipidemia. She holds both B.Pharm and M.Pharm degrees from Birla Institute of Technology, Mesra, where she consistently performed well and earned multiple academic recognitions. Professionally, she has worked as an Assistant Professor at Arya College of Pharmacy and as a Trainee Scientist II at Torrent Pharmaceuticals, gaining hands-on experience in regulatory affairs and pharmaceutical research. Her industrial exposure at Caplet India and Panacea Biotech has strengthened her understanding of QA, QC, production, packaging, and large-scale formulation processes. She is proficient with regulatory and technical tools such as SPL, eCTD, Rosetta, TITD, and Lorenz, and has practical experience with key analytical and formulation equipment. Beyond academics and industry, she is an active and creative individual who enjoys poetry writing, cooking, dancing, and contributing to cultural and social initiatives.
Prof. (Dr.) Gourishankar Birtia is currently working as Professor and Head, Department of Pharmaceutics (M.Pharm), Sanaka Educational Trust’s Group of Institutions, Malandighi, Durgapur, West Bengal, India, with over 15 years of combined teaching, research, and pharmaceutical industry experience. He holds B.Pharm, M.Pharm, MBA in Pharmaceutical Management, and Ph.D. degrees. His areas of interest include formulation development, novel drug delivery systems, dissolution studies, and pharmaceutical technology, with practical exposure to industry-oriented research and development. He has published numerous research papers, patents, and book chapters in reputed national and international publications and has guided many undergraduate and postgraduate students. He is actively involved in teaching, research, academic mentoring, and industry–academia collaboration.
Dr. Sripathi Srinivas is an accomplished academician serving as an Associate Professor in the Department of Pharmaceutics at Surabi Dayakar Rao College of Pharmacy, Gajwel, Siddipet. He has significant experience in teaching and guiding undergraduate and postgraduate students in pharmaceutical sciences. His areas of expertise include formulation development, drug delivery systems, and pharmaceutical technology. Dr. Srinivas is actively involved in research activities and has contributed to various scholarly publications. He is dedicated to enhancing students’ understanding through practical and research-oriented approaches. His commitment to academic excellence and innovation makes him a valuable contributor to the field of pharmaceutics.
Dr Nayyar Parvez is working as Professor in the School of Pharmacy, Sharda University, Greater Noida, Uttar Pradesh. He has 24 years of Teaching & Research Experience at National & International Levels. He has completed his M.Pharm & PhD in Pharmaceutics from Jamia Hamdard, New Delhi. He was awarded GOLD MEDAL in M. Pharm (Pharmaceutics). His Research area is Formulation and Evaluation of Conventional & NDDS using synthetic and natural Polymers, Bioavailability and Bioequivalence studies of conventional and sustained release dosage forms. He was awarded Ranbaxy Research Fellowship also. He has published 72 research papers in National and International journals and presented papers in international and national conferences. He has organized various conferences and workshops. He is a life member of various professional bodies like IPA, IPGA, and ISTE, APP. He has Guided 16 M. Pharm students and 7 Ph.D. students are currently enrolled and two students have completed their Ph.D. under his guidance. He has published 8 patents and 03 patents has been granted. He has also published 5 books and 6 Book chapters. He is actively involved in reviewing research papers and serving as editor and Editor in chief for National and international journals.
