Clinical Trials and Human Research: A Practical Guide to Regulatory Compliance
| Author | : | |
| Rating | : | 4.64 (503 Votes) |
| Asin | : | 0787965707 |
| Format Type | : | paperback |
| Number of Pages | : | 656 Pages |
| Publish Date | : | 2013-09-27 |
| Language | : | English |
DESCRIPTION:
The practical insights found in this volume are not found in other books on the subject. 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. This easy-to-read reference book provides a practical approach for dealing with the legal and regulatory compliance issues involved in human research. Clinical Trials and Human Research is a practical tool to help anyone involved in clinical research.. In addition, insurance, quality management, accreditation, and risk management are topics examined in the book
Clinical TrialsRegulatory Compliance Psych Major I like the way this book makes IRB's, HIPAA, and research policies easy to understand. It also offers great references of resources within the government agencies that enforce these Rules.
"Ideal for anyone who wants a comprehensive understanding of clinical research…" (Journal of Clinical Research Best Practices)
Fay A. is an affiliate associate professor in the Department of Legal Medicine at Virginia Commonwealth University's School of Medicine. Rozovsky has served as the administrator of an Institutional Review Board and is a member of human research committees in the United States and Canada. C. Rozovsky, J.D., M.P.H. Adams, J.D., L.L.M., is an attorney in Richmond, Virginia, where he specializes in defending healthcare providers and patient care issues. Rozovsky,Fay A. . M