Pharmacovigilance

Written by multidisciplinary experts in the fields of pharmaceutical and patient safety, <i>Pharmacovigilance: A Practical Approach, Second Edition</i>, provides a <b>succinct, easy-to-digest overview</b> of an increasingly critical area of medical safety. From cover to cover, this concise resource offers <b>essential information for physicians and other health care professionals</b>, clinical researchers, and regulators who need a comprehensive, up-to-date source of information on the principles and practice of pharmacovigilance.<ul><li>Presents <b>vital, easy-to-read, cutting-edge information</b> on patient safety, the pharmacology regulatory landscape, and the current and future use of digital technologies</li><li>Provides <b>up-to-date coverage of hot topics in the field</b>, including pharmacodynamic and safety precision medicine, immunogenicity, vaccine hesitancy and safety, genetic toxicology, and adverse events</li><li>Contains <b>new chapters</b> on pre-clinical safety assessment, pharmacogenetics, first-in human trials, product aggregate safety assessment, data monitoring committees, and more</li><li>Offers new and expanded coverage of pharmacovigilance in early pre-clinical drug development through post-marketing surveillance, as well as a <b>blueprint for training</b> future pharmacovigilance professionals</li><li>Includes <b>real-world case studies</b> to ensure content is relevant and applicable to everyday practice</li><li>Discusses <b>a range of topics across disciplines</b> and how they relate to pharmacovigilance, including behavioral science, patient perspectives, and risk communication</li><li><b>An eBook version is included with purchase.</b> The eBook allows you to access all of the text, figures and references, with the ability to search, customize your content, make notes and highlights, and have content read aloud. Additional digital ancillary content may publish up to 6 weeks following the publication date</li></ul>