Clinical Trials and Human Research: A Practical Guide to Regulatory Compliance,Used

Clinical Trials and Human Research: A Practical Guide to Regulatory Compliance,Used

In Stock
SKU: SONG0787965707
Brand: Wiley
Regular price$34.30
Quantity
Add to wishlist
Add to compare

Processing time: 1-3 days

US Orders Ships in: 3-5 days

International Orders Ships in: 8-12 days

Return Policy: 15-days return on defective items

Payment Option
Payment Methods

Help

If you have any questions, you are always welcome to contact us. We'll get back to you as soon as possible, withing 24 hours on weekdays.

Customer service

All questions about your order, return and delivery must be sent to our customer service team by e-mail at yourstore@yourdomain.com

Sale & Press

If you are interested in selling our products, need more information about our brand or wish to make a collaboration, please contact us at press@yourdomain.com

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: What is the main focus of 'Clinical Trials and Human Research'? A: The book focuses on providing a practical approach to regulatory compliance in human research, covering essential topics such as consent, confidentiality, and the role of the investigator.
  • Q: Who is the author of this book? A: The author of 'Clinical Trials and Human Research' is Fay A. Rozovsky.
  • Q: What type of binding does this book have? A: This book is bound in hardcover.
  • Q: How many pages are in this book? A: The book contains a total of 656 pages.
  • Q: When was 'Clinical Trials and Human Research' published? A: The book was published on June 10, 2003.
  • Q: Is this book suitable for beginners in clinical research? A: Yes, the book is designed to be easy to read and provides practical insights, making it suitable for both beginners and experienced professionals in clinical research.
  • Q: Does this book discuss risk management in clinical trials? A: Yes, risk management is one of the key topics examined in the book.
  • Q: What condition is the book in? A: The book is listed as 'New'.
  • Q: Can this book help with Institutional Review Board requirements? A: Yes, it covers the role of the Institutional Review Board and offers strategies for compliance.
  • Q: Is this book part of a specific category? A: Yes, it falls under the category of Medical Law & Legislation.

Recently Viewed