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Considerations for applying bioethics norms to a biopharmaceutical industry setting

机译:将生物伦理规范应用于生物制药行业环境的考虑因素

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The biopharmaceutical industry operates at the intersection of life sciences, clinical research, clinical care, public health, and business, which presents distinct operational and ethical challenges. This setting merits focused bioethics consideration to complement legal compliance and business ethics efforts. However, bioethics as applied to a biopharmaceutical industry setting often is construed either too broadly or too narrowly with little examination of its proper scope. Any institution with a scientific or healthcare mission should engage bioethics norms to navigate ethical issues that arise from the conduct of biomedical research, delivery of clinical care, or implementation of public health programs. It is reasonable to assume that while bioethics norms must remain constant, their application will vary depending on the characteristics of a given setting. Context “specification” substantively refines ethics norms for a particular discipline or setting and is an expected, needed and progressive ethical activity. In order for this activity to be meaningful, the scope for bioethics application and the relevant contextual factors of the setting need to be delineated and appreciated. This paper defines biopharmaceutical bioethics as: the application of bioethics norms (concepts, principles, and rules) to the research, development, supply, commercialization, and clinical use of biopharmaceutical healthcare products. It?provides commentary on this definition, and presents five contextual factors that need to be considered when applying bioethics norms to a biopharmaceutical industry setting: (1) dual missions; (2) timely and pragmatic guidance; (3) resource stewardship; (4) multiple stakeholders; and (5) operational complexity. Understanding the scope of the biopharmaceutical enterprise and contextual factors of a biopharmaceutical industry setting is foundational for the application of bioethics norms. Establishing a common language and approach for biopharmaceutical bioethics will facilitate breadth and depth of discussion and subsequent implementation to benefit patients, the healthcare system and society.
机译:生物制药行业在生命科学,临床研究,临床护理,公共卫生和业务方面运作,这呈现出独特的运营和道德挑战。此设定的优点是重点的生物伦理思考虑,以补充法律遵守和商业道德工作。然而,应用于生物制药行业环境的生物伦理经常被过于广泛或过于狭隘地解释其适当的范围。任何具有科学或医疗保健代表团的机构都应聘请生物伦理规范,以导致生物医​​学研究,临床护理或实施公共卫生计划的行为中产生的道德问题。假设是合理的,虽然生物伦理规范必须保持不变,但其应用程序将根据给定设置的特征而变化。背景信息“规范”实质地改进特定纪律或环境的道德规范,是预期的,需要和逐步的道德活动。为了使这项活动有意义,需要划算和赞赏地区的生物伦理应用和相关的环境的相关上下文因素。本文定义了生物制药生物伦理学::将生物伦理规范(概念,原则和规则)应用于生物制药医疗产品的研究,开发,供应,商业化和临床应用。它是关于这种定义的评论,并在将生物伦理规范应用于生物制药行业时,呈现五个需要考虑的内容因素:(1)双重任务; (2)及时和务实的指导; (3)资源管理; (4)多个利益相关者; (5)操作复杂性。了解生物制药企业的范围和生物制药行业环境的上下文因素为生物伦理规范的应用是基础的。建立一种常识和生物制药生物伦理的方法将促进宽度和深度的讨论和随后的实施,使患者受益,医疗保健系统和社会。

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