Developing Solid Oral Dosage Forms is intended for pharmaceutical professionals engaged in research and development of oral dosage forms. It covers essential principles of physical pharmacy, biopharmaceutics and industrial pharmacy as well as various aspects of state-of-the-art techniques and approaches in pharmaceutical sciences and technologies along with examples and/or case studies in product development. The objective of this book is to offer updated (or current) knowledge and skills required for rational oral product design and development. The specific goals are to provide readers with: - Basics of modern theories of physical pharmacy, biopharmaceutics and industrial pharmacy and their applications throughout the entire process of research and development of oral dosage forms - Tools and approaches of preformulation investigation, formulation/process design, characterization and scale-up in pharmaceutical sciences and technologies - New developments, challenges, trends, opportunities, intellectual property issues and regulations in solid product development - The first book (ever) that provides comprehensive and in-depth coverage of what's required for developing high quality pharmaceutical products to meet international standards - It covers a broad scope of topics that encompass the entire spectrum of solid dosage form development for the global market, including the most updated science and technologies, practice, applications, regulation, intellectual property protection and new development trends with case studies in every chapter - A strong team of more than 50 well-established authors/co-authors of diverse background, knowledge, skills and experience from industry, academia and regulatory agencies

Selected peer reviewed full text papers from the 3rd International Conference and Exhibition on Pharmaceutical Sciences and Technology (PST 2020) Selected, peer-reviewed papers from the 3rd International conference and exhibition on Pharmaceutical Sciences and Technology (PST 2020), May 19-20, 2020, Bangkok , Thailand

Written for all pediatric clinicians and students, Problems in Pediatric Drug Therapy is an authoritative, well-referenced, and accessible source of essential information on the use and effects of drugs in infants and children. Twenty widely published clinicians, educators, and researchers from pharmacy, medicine, and nursing have authored 14 chapters, each dealing with a major, potentially problematic area of pediatric drug therapy. Building on the well-received previous editions -- the third edition was named an American Journal of Nursing Book of the Year in the category of pediatric nursing -- the fourth edition focuses on the key concerns in pediatric drug therapy today: drug administration, pharmacokinetics, drugs as teratogens and fetotoxins, excretion of drugs into breast milk, pediatric poisoning, adverse reactions, drug interactions, drug abuse, IV drugs, and immunizations. Two new chapters cover the increasingly important areas of pediatric antineoplastic therapy and pharmacogenetics. The concluding two hallmark chapters on dosing in neonates and in infants, children, and adolescents, respectively, have been expanded and updated to reflect current trends in drug use.

How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval uses a practical and hands-on approach to cover the development process of solid oral dosage forms in one single source. The book details all of the necessary steps from formulation through the post-approval phase and contains industry case studies, real world advice, and troubleshooting tips. By merging the latest scientific information with practical instructions, this book provides pharmaceutical scientists in formulation research and development with a concrete look at the key aspects in the development of solid oral dosage forms. - Focuses on important topics, such as robustness, bioavailability, formulation design, continuous processing, stability tests, modified release dosage forms, international guidelines, process scale-up, and much more - Part of the Expertise in Pharmaceutical Process Technology series edited by Michael Levin - Discusses common, real-world problems and offers both theoretical and practical solutions to these everyday issues