Ethical and Regulatory Aspects of Clinical Research: Readings and Commentary

Looking to meet the ethical and regulatory requirements of clinical research? Look no further! Introducing Ethical and Regulatory Aspects of Clinical Research: Readings and Commentary, the ultimate guide for investigators funded by the National Institutes of Health. This comprehensive book has been specially designed to help you navigate the complex world of clinical research ethics.

The editors, who have extensive experience teaching courses at NIH, bring you a wealth of knowledge and insights. From the history of human subjects research to the latest guidelines, this book covers it all. Gain a deep understanding of the various stages and components of the clinical trial process, including trial design, participant recruitment, informed consent, studying special populations, and conducting international research.

But that's not all! Ethical and Regulatory Aspects of Clinical Research goes beyond the basics and tackles important topics like conflicts of interest, scientific misconduct, and challenges to the IRB system. The inclusion of sample informed consent forms in the appendix further enhances the practicality of this book.

Designed to be used in undergraduate courses on research ethics, as well as in schools of medicine and public health, this book is essential for students and professionals involved in clinical research. Whether you're new to the field or seeking to enhance your expertise, Ethical and Regulatory Aspects of Clinical Research is your go-to resource.

Don't miss out on this opportunity to stay ahead of the game. Get your copy today and take the first step towards mastering ethical and regulatory aspects of clinical research! Order now.