Provides a comprehensive and thorough reference on the basics and practices of clinical trials Includes chapters on hot topics like: adverse event reporting (AER) systems,... Læs mere
This book is a one-stop compendium of up-to-date concepts, approaches, methodologies, and limitations in drug development and therapeutics. It provides... Læs mere
This handbook features contributions from a team of expert authors representing the many disciplines within science, engineering, and... Læs mere
With its coverage of Food and Drug Administration regulations, international regulations, good manufacturing practices, and process... Læs mere
This book provides drug safety and toxicology scientists with practical guidance for testing and determining the effectiveness and safety of a new drug... Læs mere
This book gives the professional pharmaceutical scientist a basic and comprehensive tool to facilitate the preclinical development... Læs mere
Pharmaceutical Manufacturing Handbook covers a range of topics to help professionals better understand the methods used in the pharmaceutical manufacturing, pharmaceutical engineering, and process engineering fields.