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Clinical Trials And Human Research: A Practical Guide To Regulatory Compliance,New
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This Easytoread Reference Book Provides A Practical Approach For Dealing With The Legal And Regulatory Compliance Issues Involved In Human Research. Covering A Broad Range Of Topics, Such As Consent, Confidentiality, Subject Recruitment And Selection, The Role Of The Investigator And Institutional Review Board, It Offers Timely And Useful Strategies For Achieving Regulatory Compliance While Reducing Liability. In Addition, Insurance, Quality Management, Accreditation, And Risk Management Are Topics Examined In The Book. The Practical Insights Found In This Volume Are Not Found In Other Books On The Subject. Clinical Trials And Human Research Is A Practical Tool To Help Anyone Involved In Clinical Research.
⚠️ WARNING (California Proposition 65):
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 this book have? A: This book has six hundred fifty-six pages. It provides extensive coverage of regulatory compliance in human research.
- Q: What is the binding type of this book? A: The binding type of this book is hardcover. This ensures durability and longevity for frequent use.
- Q: What are the dimensions of this book? A: The dimensions of this book are seven point twenty-four inches in length, one point forty-seven inches in width, and ten point twenty-six inches in height. These measurements make it a manageable size for reading.
- Q: Who is the author of this book? A: The author of this book is Fay A. Rozovsky. She offers valuable insights into medical law and legislation.
- Q: What category does this book fall under? A: This book falls under the category of Medical Law & Legislation. It is designed for professionals involved in clinical trials and human research.
- Q: Is this book suitable for beginners? A: Yes, this book is suitable for beginners. It provides a practical approach to understanding regulatory compliance in an accessible manner.
- Q: Can this book help with consent issues in research? A: Yes, this book addresses consent issues in research. It offers strategies to effectively manage legal and ethical considerations.
- Q: Who would benefit from reading this book? A: Anyone involved in clinical research, including investigators and institutional review board members, would benefit from this book. It provides practical insights not found in other resources.
- Q: Is this book helpful for understanding risk management? A: Yes, this book covers risk management. It discusses strategies for reducing liability in clinical research settings.
- Q: How should I care for this book? A: To care for this book, keep it in a cool, dry place and avoid exposure to direct sunlight. This will help preserve the binding and pages.
- Q: Can this book be used as a reference for legal compliance? A: Yes, this book can be used as a reference for legal compliance in human research. It offers practical guidance on navigating complex regulations.
- Q: What if the book arrives damaged? A: If the book arrives damaged, you should contact the seller for a return or exchange. Most sellers have policies in place for damaged items.
- Q: Does this book cover insurance topics? A: Yes, this book covers insurance topics related to clinical trials. It examines how insurance impacts regulatory compliance.
- Q: Is this book available in other formats? A: No, this book is only available in hardcover format. This choice enhances its durability for professional use.
- Q: Can I use this book for accreditation purposes? A: Yes, you can use this book for accreditation purposes. It discusses quality management and accreditation in clinical research.
- Q: How often should I refer to this book? A: You should refer to this book regularly for updates on regulatory compliance. It serves as a valuable ongoing resource.