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Pharmaceutical Preformulation and Formulation
Collects discussions from more than 30 noted specialists on topics such as quality control, experimental formulations, pharmaceutical ingredients, conventional and modified-release products and bioequivalence. This title considers key elements in the formulation of generic drug products including availability of raw materials and chemical purity.
Pharmaceutical Product Development
Generic Drug Product Development
Oral Lipid-Based Formulations
Pharmaceutical Photostability and Stabilization Technology
Modified-Release Drug Delivery Technology
Supplying a framework for employing simulation as an experiment, this book discusses how to clinically trial designs according to their probability for success. It gives techniques to define distributions of virtual subjects' characteristics, and methods to determine the sensitivity of the trial design.
Provides an coverage of the development, preparation, and application of topical and transdermal therapeutic systems. This book discusses the bioequivalence of dermatological and transdermal dosage forms. It explores the biochemistry and treatment of skin diseases, the structure and function of the skin, and more.
This book brings together an up-to-date account of instructions in the chemical and biological methods of analysis for antibiotics. It is helpful for all scientific workers in the diversified community of industrial, medical, academic, and governmental antibiotic laboratories.
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 nutrition. It is intended for nutritionists and clinical investigators concerned with interpretation of aberrant effects of therapeutic drugs.
Injectable Dispersed Systems
Analyses construction of experiments, focusing on variables, models and other topics. This book examines the concepts and theoretical issues, methodologies for experiment and measurement, and health applications of emulsions and dispersions - describing formulation problems and identifying carriers for the delivery or targeting of drugs.
This book provides comprehensive information on pharmaceutical dissolution technology. It serves as an invaluable guide to aid the pharmacy professional in selecting and utilizing the available means in overcoming problems in design and development of better dosage forms.
Addressing issues at the forefront of interest for the Clinical Trial Materials Professional (CTMP), this Second Edition highlights the most critical concepts related to the planning, manufacturing, packaging, labeling, distribution, reconciliation, and quality and regulatory control of clinical trial materials. It offers authoritative chapters by esteemed researchers and consultants in industry on the current and evolving state of clinical supplies operations. Tracking emerging trends and the development of new technologies, this Second Edition helps the CTMP operate effectively in the international sphere and reviews regulatory processes for drug approvals in the United States and Europe.
Provides information on containment processes. This book reviews the historical context, definition, evolution, and application of containment technology, analyzes a variety of containment techniques in construction, and examines "people protection" vs. "product protection" and the role of source-contamination in each.
Describes the statistical planning and design of pharmaceutical experiments, covering all stages in the development process. Comparing the advantages and disadvantages of specific techniques, this book shows how to overcome pharmaceutical, technological, and economic constraints on experiment design.
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