Gør som tusindvis af andre bogelskere
Tilmeld dig nyhedsbrevet og få gode tilbud og inspiration til din næste læsning.
Ved tilmelding accepterer du vores persondatapolitik.Du kan altid afmelde dig igen.
Suitable for researchers and students in pharmacology and related fields, this title explains the techniques for investigating the absorption, distribution, metabolism, and excretion of test compounds using laboratory animals. It describes types of experiments, study design, and animal preparation and maintenance.
The third edition of this text contains additional chapters which cover troubleshooting procedures, validation in contract manufacturing and current harmonization trends.
Clean-In-Place for Biopharmaceutical Processes
Explores the various aspects of multiparticulate dosage form development, assessing the in vivo behaviour and performance of multiparticulates as well as comparing their market position to other dosage forms. Alternative pelletization techniques are comprehensively discussed.
This book serves as a formulation and processing guide during the development of pelletized dosage forms. It provides the pharmaceutical technologist with basic information about the design aspects of the relevant processing equipment.
Preformulation in Solid Dosage Form Development
Surveys emerging trends, concepts, and procedures used in the characterization and control of contaminants; the sterile production of traditional drugs and biologics; the design, construction, and validation of parenteral facilities; and the monitoring of clean environments.
Features the findings surrounding the physicochemical aspects of surfactant and polymer systems to facilitate the design and understanding of drug delivery formulations. This book covers the basics of surfactant and polymer surface activity and self-assembly, the various types of structures formed by such compounds, and their use in drug delivery.
Addressing concerns for patient welfare while protecting producer reputation, and providing a database for formulation of other products. This book gives fundamental theory and practical advice on drug product stability in scientific, technical, and regulatory environments, covering development of indicating assays, computer use, and others.
Explores the principles, instrumentation, processes, and programs of pharmaceutical solid science as well as fresh aspects on one-component systems, micromeritics, polymorphism, solid-state stability, cohesion, powder flow, blending, single-unit sustained release, and tablet coating.
Pharmaceutical Powder Compaction Technology
Sterile Drug Products
Freeze-Drying/Lyophilization of Pharmaceutical and Biological Products
Pharmaceutical Stress Testing
Drug Delivery Nanoparticles Formulation and Characterization
Generic Drug Product Development
Biodrug Delivery Systems
Drug Stereochemistry
Proteins and Peptides
Active Pharmaceutical Ingredients
Pharmaceutical Statistics
Tilmeld dig nyhedsbrevet og få gode tilbud og inspiration til din næste læsning.
Ved tilmelding accepterer du vores persondatapolitik.