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A comprehensive treatment of the science, technology, and regulation of rate-controlled administration of therapeutic agents, with coverage of the bas...Savoir plus
The preparation of sterile products using aseptic processing is considered perhaps the most critical process in the pharmaceutical industry and has wi...Savoir plus
Thoroughly revised to include the latest industry developments, the Second Edition presents a comprehensive overview of computer validation and verifi...Savoir plus
Biodrug Delivery Systems: Fundamentals, Applications and Clinical Development presents the work of an international group of leading experts in drug d...Savoir plus
This book provides insight into the world of pharmaceutical quality systems and the key elements that must be in place to change the business and orga...Savoir plus
This invaluable reference presents a comprehensive review of the basic methods for characterizing bioadhesive materials and improving vehicle targetin...Savoir plus
With the advent of analytical techniques and capabilities to measure particle sizes in nanometer ranges, there has been tremendous interest in the use...Savoir plus
This fully revised and updated third edition of Pharmaceutical Inhalation Aerosol Technology encompasses the scientific and technical foundation for t...Savoir plus
When a biological drug patent expires, alternative biosimilar products are developed. The development of biosimilar products is complicated and involv...Savoir plus
A practical guide for chemists in the pharmaceutical industry to making automated analyses of drugs that will meet the standards of regulatory agencie...Savoir plus
Project managers in drug development are the driving force behind the coordination of efforts. This book provides a practical reference for project ma...Savoir plus
The assessment of bioequivalence is an important process whereby the bioavailability of a generic drug product is compared with its brand-name counter...Savoir plus
Since sterile filtration and purification steps are becoming more prevalent and critical within medicinal drug manufacturing, the third edition of Fil...Savoir plus
This work describes all known assays used to discover new glycopeptide antibiotics. It discusses practical techniques for screening, isolating and ana...Savoir plus
This blue-chip guide adds quality to the pharmaceutical clinical development process by detailing the need for, and stressing the importance of, an in...Savoir plus
Aimed at those already involved in drug development or those considering entering the field, Clinical Drug Trials and Tribulations, Second Edition com...Savoir plus
Addressing issues at the forefront of interest for the Clinical Trial Materials Professional (CTMP), this Second Edition highlights the most critical ...Savoir plus
Oral lipid-based formulations are attracting considerable attention due to their capacity to facilitate gastrointestinal absorption and reduce or elim...Savoir plus
For researchers and students in pharmacology and related fields, explains the standard techniques for investigating the absorption, distribution, meta...Savoir plus
This book is devoted to the effects of food and of nutrient intake on the disposition of foreign compounds, and discusses effects of drugs on nutritio...Savoir plus
This book provides a thorough reference on Good Clinical Practice (GCP) which is the international ethical, scientific and practical standard to which...Savoir plus
Analyzes construction of experiments, focusing on variables, models, matrices, and reproducibility. This timely reference systematically examines the ...Savoir plus
With the advent of analytical techniques and capabilities to measure particle sizes in nanometer ranges, there has been tremendous interest in the use...Savoir plus
During the last two decades, the pharmaceutical industry has been under pressure to reduce development costs and the time needed to bring drugs to mar...Savoir plus