Conceived and edited by Nigel Dent and Ramzan Visanji, this book explores how to conduct studies and ensure that the studies are guided by GCPs and are in compliance with regulations. Comprehensive in scope, it provides the scientific, biological, and regulatory background invaluable to teachers, researchers, and regulatory affairs staff, as well as those directly involved in clinical trials.
The chapters can be read sequentially for a comprehensive view or individually for coverage of particular topics and issues as needed. Drawing directly from the in-the-trenches experience of the editors and chapter authors, this book contains strategies that ensure avoidance of common pitfalls.
The chapters can be read sequentially for a comprehensive view or individually for coverage of particular topics and issues as needed. Drawing directly from the in-the-trenches experience of the editors and chapter authors, this book contains strategies that ensure avoidance of common pitfalls.
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