Bøger i Drugs and the Pharmaceutical Sciences serien

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.

Nanoparticulate Drug Delivery Systems

Pharmaceutical Product Development

Modified-Release Drug Delivery Technology

Modified-Release Drug Delivery Technology

Pharmaceutical Project Management

Generic Drug Product Development

Dermal Absorption and Toxicity Assessment

Oral Lipid-Based Formulations

Dose Optimization in Drug Development

Pharmaceutical Photostability and Stabilization Technology

Modified-Release Drug Delivery Technology

Nanoparticle Technology for Drug Delivery

Microencapsulation

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

Percutaneous Absorption

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.

Reviews important colloidal drug delivery systems, that include nanoparticles, liposomes, niosomes, microemulsions and ointments. This book provides over 1000 bibliographic citations, as well as tables, drawings, equations and photographs.

A practical guide for chemists in the pharmaceutical industry to making automated analyses of drugs that meet the standards of regulatory agencies. It reviews the standard techniques of high-performance liquid chromatography, specialized detection methods, and automation in pharmaceutical analysis.

Describes the bases for developing dosage forms for use in animals, highlighting the data necessary to meet regulatory approval. This title demonstrates the successful characterization, control, and registration of fresh veterinary medicines. It is suitable for pharmaceutical, animal, and quality control scientists.

Reviews the history, regulatory status, pharmacopeial specifications, and harmonization of pharmaceutical excipients. This book provides an scientific basis for safety evaluation and risk assessment. It identifies the differences between excipients, food ingredients, and drug products; and more. It is for pharmacists; toxicologists; and others.