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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