This book focuses on the practical application of good clinical
practice (GCP) fundamentals and provides insight into roles and
responsibilities included in planning, executing, and analyzing
clinical trials. The authors describe the design of quality into
clinical trial planning and the application of regulatory,
scientific, administrative, business, and ethical considerations.
Describes the design of quality into the clinical trial planning
Has end-of-chapter questions and answers to check learning and
comprehension Includes charts that visually summarize the content
and allow readers to cross-reference details in relevant chapters
Offers a companion website containing supplemental training
resources
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