This easy-to-read 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.