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首页> 外文期刊>Therapeutic innovation & regulatory science. >Patient Engagement at a Tipping Point-The Need for Cultural Change Across Patient, Sponsor, and Regulator Stakeholders: Insights From the DIA Conference, 'Patient Engagement in Benefit Risk Assessment Throughout the Life Cycle of Medical Products'
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Patient Engagement at a Tipping Point-The Need for Cultural Change Across Patient, Sponsor, and Regulator Stakeholders: Insights From the DIA Conference, 'Patient Engagement in Benefit Risk Assessment Throughout the Life Cycle of Medical Products'

机译:病人参与的转折点-跨患者,申办者和监管者的利益相关者的文化变革的需求:DIA会议的见解,“在医疗产品整个生命周期中的患者参与利益风险评估”

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摘要

Benefit-risk assessment is the foundation for decision making throughout the life cycle of medical products. Because patients are the beneficiaries of the efficacy of medical treatments and also bear their possible risks, their perspectives and judgments about value and the relative importance of benefits and risks should be at the heart of the medical decision-making process. Patient engagement is now at a tipping point; there have been a growing number of patient engagement initiatives over the past several years, but there remains the need for a common language, alignment on engagement approaches and best practices, and a shared vision regarding a desired future state. This article discusses insights gleaned from the DIA conference, "Patient Engagement in Benefit-Risk Assessment throughout the Life Cycle of Medical Products" (September 20 15). It highlights the changes that will need to occur within the patient, medical-product sponsor, and regulatory cultures in order for patient engagement to become integrated into the medical-product development process and life cycle maintenance. Furthermore, it emphasizes that reaching the desired future state will require a conscious commitment from all stakeholders to work collaboratively to develop shared solutions and to map a common path forward.
机译:利益风险评估是整个医疗产品生命周期决策的基础。因为患者是医疗功效的受益者,并且还承担着可能的风险,所以他们对价值以及利益和风险的相对重要性的看法和判断应该成为医疗决策过程的核心。现在,患者参与正处于转折点。在过去的几年中,越来越多的患者参与计划开始了,但是仍然需要一种通用的语言,对参与方法和最佳实践的统一以及对理想未来状态的共同愿景。本文讨论了DIA会议上收集的见解,即“在医疗产品整个生命周期中的患者参与风险评估的过程”(9月20日至15日)。它着重说明了患者,医疗产品赞助商和法规文化内部将需要发生的变化,以使患者参与度能够融入医疗产品开发过程和生命周期维护中。此外,它强调要达到理想的未来状态,将需要所有利益相关者的自觉承诺,以共同努力以开发共享的解决方案并规划共同的前进道路。

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