Regulatory Investigations: Regulators, Regulatees and the Public Interest.

IF 0.6 Q2 LAW
Journal of Law and Medicine Pub Date : 2022-12-01
Arie Freiberg
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引用次数: 0

Abstract

The potential for adverse consequences of investigations by a regulatory authority into complaints made against a person whom it regulates raises important questions about how regulators or similar bodies are, or should be, held accountable for their actions. This article examines the legal duties or other obligations that a regulator of health practitioners owes to people it regulates as well as to those who make complaints or submit notifications and to the public at large. It raises the general question of what duties or obligations any regulator or similar body with investigatory or coercive powers owes to persons arising out of its investigations. It finds that although they do not have a legal duty of care to a regulatee to protect them from harm, there may be other reasons why a regulator may want to consider the welfare of those whom it regulates as well as other affected parties.

监管调查:监管者、被监管者和公共利益。
监管机构对其监管对象的投诉进行调查可能产生不利后果,这引发了一个重要问题,即监管机构或类似机构如何(或应该)对其行为负责。本文探讨了医疗从业人员监管机构对其监管的人、对提出投诉或提交通知的人以及对广大公众应承担的法律责任或其他义务。它提出了一个普遍的问题,即任何具有调查或强制权力的监管机构或类似机构对其调查产生的人负有什么责任或义务。研究发现,尽管监管者没有保护被监管者免受伤害的法律义务,但可能有其他原因可以解释为什么监管者可能想要考虑被监管者以及其他受影响方的福利。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
63
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