Human subjects research regulation: perspectives on the future
本书探讨美国人类受试者研究监管法规（共同规则）的拟议改革，旨在推动围绕风险导向监管和生物样本研究挑战的对话。
This book is the 43rd in a series entitled ‘Basic bioethics’, and is intended to make work in bioethics accessible to a broad audience. This volume looks at the regulations safeguarding research involving human participants, and explores the legislative framework governing research in the US, in particular the ‘Common Rule for the Protection of Human Subjects’. The reason for this focus is that there have been a number of proposed changes (described within the Advanced Notice for Proposed Rulemaking, or ANPRM) which aim to take a risk-based approach to targeting regulatory oversight, as well as modifying regulations to keep pace with research, particularly regarding multi-site trials and the challenges facing research involving use of biological specimens. One of the points made in the introduction is that at the time of writing (late 2013) little progress had been made in terms of this legislative review. Indeed, at the time of writing this review, the process is far from complete. The aim of the book, therefore, is to stimulate dialogue around the proposed changes.