Pharmaceutical Development Series
The Pharmaceutical Development Series is an all-inclusive resource relating to the development of pharmaceuticals for pharmaceutical scientists, pharmaceutical engineers and students. The reader will find answers to specific questions, to problems, or a concise introduction to a topic and references to authoritative treatment in the literature. This Series provides the readers a quick, easily accessible, and reliable source of information to pharmaceutical development.
The Pharmaceutical Development Series has been developed with the awareness that the discovery and development of new drugs and therapies combine a broad range of scientific principles—it recognizes the interdisciplinary nature of the pharmaceutical industry and the needs of the professionals in the field to have a broad base of knowledge in a variety of sciences. This Series provides thorough foundations in numerous areas of pharmaceutical development--covering everything from drug discovery, drug development, R& D, pharmacokinetics, pharmacology, safety, formulation, regulatory requirements, quality assurance, quality control to drug labeling.
Pharmaceutical Development Series (12)
• Helps readers solve scientific, technical, and regulatory issues in preclinical safety assessment and early clinical drug development
• Explains scientific and philosophical bases for evaluation of specific concerns – including local tissue tolerance, target organ toxicity and carcinogenicity, developmental toxicity Read More
Providing both understanding and guidance in characterizing potential drugs and their production and synthesis, Development of Therapeutic Agents Handbook gives professionals a basic tool to facilitate research and development within this challenging process. This comprehensive text brings together, in one resource, a compendium of concepts, approaches Read More
Clinical trials are arguably the most important steps in proving drug effectiveness and safety for public use. They require intensive planning and organization and involve a wide range of disciplines: data management, biostatistics, pharmacology, toxicology, modeling and simulation, regulatory monitoring, ethics, and particular issues for given disease areas. Read More
Drug Safety Evaluation
Shayne Cox Gad
The updated and expanded safety guide to all aspects of the drug development process
Drug Safety Evaluation, Second Edition presents an all-inclusive, practical guide for those who are responsible for ensuring the safety of drugs and biologics for patients, for health care providers, for those involved in the manufacture of medicinal products, and for all those who need to understand how the safety Read More
Following this book's step-by-step guidance, you can successfully initiate and complete critical phases of preclinical drug development. The book serves as a basic, comprehensive reference to prioritizing and optimizing leads, dose formulation, ADME, pharmacokinetics, modeling, and regulations. This authoritative, easy-to-use resource covers all the issues that need Read More
Following this book's step-by-step guidance, you can successfully initiate and complete critical phases of preclinical drug development. The book serves as a basic,comprehensive reference to prioritizing and optimizing leads, toxicity, pharmacogenomics, modeling, and regulations. This single definitive, easy-to-use resource discusses all the issues that need consideration Read More
The Handbook of Pharmaceutical Biotechnology helps pharmaceutical scientists develop biotech drugs through a comprehensive framework that spans the process from discovery, development, and manufacturing through validation and registration. With chapters written by leading practitioners in their specialty areas, this reference: Read More
This comprehensive, practical guide presents an explanation of the latest techniques and methods in drug discovery, including: Read More