Ethical Conduct of Research in the Clinical Environment

Lori Boyd RT(R), BA, MA, EdD(c)
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Abstract

Clinical research has a long history of questionable ethical practice. Abuse of subjects and neglectful research practices have harmed individuals, groups, and the reputation of the scientific community. Policies, codes, and guidelines have been implemented and enforced as a result. To ensure ethical research practice, clinical trials and studies need to be assessed at various stages to ensure ethical design, just recruitment practices, voluntary informed consent, safe and ethical conduct, and appropriate dissemination of results. This paper identifies and explains ethical principles that apply to research. The purpose and focus of the four fundamental policy documents that inform current research practice are outlined. Ethical challenges that a researcher may face are also discussed. The requirements related to the humane use of animals for research purposes will be considered. Lastly, controversies and challenges with exporting research to developing countries will be briefly discussed.

临床环境中研究的伦理行为
长期以来,临床研究一直存在道德实践方面的问题。滥用研究对象和忽视研究实践已经损害了个人、团体和科学界的声誉。因此,政策、代码和指导方针得到了实现和执行。为了确保伦理研究实践,临床试验和研究需要在不同阶段进行评估,以确保伦理设计、公正的招募实践、自愿知情同意、安全和伦理的行为以及适当的结果传播。本文确定并解释了适用于研究的伦理原则。概述了当前研究实践的四个基本政策文件的目的和重点。研究人员可能面临的伦理挑战也进行了讨论。将考虑与为研究目的人道使用动物有关的要求。最后,将简要讨论向发展中国家出口研究的争议和挑战。
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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