Title
The Fundamentals of Clinical Research: A Universal Guide for Implementing Good Clinical Practice,Used
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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 endofchapter questions and answers to check learning and comprehension Includes charts that visually summarize the content and allow readers to crossreference details in relevant chapters Offers a companion website containing supplemental training resources
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This product may contain chemicals known to the State of California to cause cancer, birth defects, or other reproductive harm.
For more information, please visit www.P65Warnings.ca.gov.
- Q: How many pages does the book have? A: The book has five hundred forty-four pages. This provides a comprehensive guide on clinical research practices and methodologies.
- Q: What is the binding type of this book? A: This book is bound in hardcover. This ensures durability and longevity for frequent use.
- Q: Who is the author of this book? A: The author is P. Michael Dubinsky. He provides valuable insights based on his expertise in clinical research.
- Q: What is the main focus of this book? A: The book focuses on implementing good clinical practice. It emphasizes practical applications and the roles involved in clinical trials.
- Q: Is there a companion website for this book? A: Yes, there is a companion website. It offers supplemental training resources to enhance the learning experience.
- Q: How do I apply the concepts from this book? A: You can apply the concepts by following the guidelines provided for planning and executing clinical trials. The end-of-chapter questions help reinforce learning.
- Q: Are there practice questions in this book? A: Yes, there are end-of-chapter questions and answers. These help check comprehension and understanding of the material.
- Q: Is this book suitable for beginners in clinical research? A: Yes, it is suitable for beginners. The book is written to provide foundational knowledge for those new to clinical research.
- Q: Can I use this book for professional development? A: Yes, this book is ideal for professional development. It provides insights that are beneficial for both new and experienced professionals.
- Q: How do I store this book properly? A: Store this book upright on a shelf. This prevents bending and damage to the binding.
- Q: Is this book safe for all readers? A: Yes, the content is educational and suitable for all audiences interested in clinical research. It maintains a professional tone.
- Q: What topics are covered in this book? A: The book covers quality design, regulatory considerations, and ethical aspects of clinical trials. It encompasses a wide range of relevant topics.
- Q: What are the dimensions of the book? A: The book has dimensions of approximately three hundred ninety inches in length, width, and height. This makes it portable and easy to handle.
- Q: Is there any visual content in the book? A: Yes, the book includes charts that visually summarize key content. These aids enhance understanding and retention of information.
- Q: What makes this book a universal guide? A: It is considered a universal guide due to its comprehensive coverage of clinical practices applicable in various settings. It addresses multiple aspects of clinical trials.
- Q: What kind of training resources are available online for this book? A: The companion website offers supplemental training resources. These resources support the material covered in the book.