将患者的需求和观点纳入额外的风险最小化措施和其他药物警戒成果-框架和实施路线图。

IF 1.9 4区 医学 Q4 MEDICAL INFORMATICS
Linda Smeding, Robert Massouh, Farai Moyo, Marilyn Metcalf, Shannon Altimari, Ekaterina Edle von Dall'Armi, Elisa Formenti
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引用次数: 0

摘要

在药品的整个生命周期中,存在各种支持患者参与(PE)的举措和指南。而最近欧洲药品管理局关于良好药物警戒做法的指南(模块十六;修订3)强调了让患者参与制定有效风险最小化策略的重要性,缺乏支持上市许可持有人(mah)在药物警戒中系统采用PE的框架,包括风险管理系统。此外,很少有关于患者审查额外风险最小化措施材料的影响。我们提出了一个经过测试的以患者为中心的药物警戒框架,描述了可以在有效的风险最小化材料中为系统PE创建必要基础设施的关键重点领域。该框架的实施强调了合作的重要性,以推动公司在本地和全球层面以及外部的PE,因为与患者组织建立了关系,并与其他mah分享了最佳实践。因此,其他公司可以考虑将该框架作为开发以患者为中心的方法的基础,将患者的声音整合到药物警戒交付成果中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Incorporating Patient Needs and Perspectives in Additional Risk Minimization Measures and Other Pharmacovigilance Deliverables - A Framework and Implementation Roadmap.

Various initiatives and guidelines exist to support patient engagement (PE) throughout the lifecycle of a medicinal product. While the recent European Medicines Agency guideline on good pharmacovigilance practices (Module XVI; Revision 3) reinforces the importance of involving patients to create effective risk minimization strategies, frameworks supporting the systematic adoption of PE by Marketing Authorization Holders (MAHs) across pharmacovigilance, including the risk management system, are lacking. Furthermore, little is presented on the impact of patient review of additional risk minimization measures materials. We present a tested Pharmacovigilance Patient Centricity Framework describing key focus areas that can create the necessary infrastructure for systematic PE in effective risk minimization materials. Implementation of this framework highlighted the importance of collaboration to drive PE across the company at both local and global level, and externally, as relationships are established with patient organizations and best practices are shared with other MAHs. Therefore, this framework can be considered by other companies as a basis for developing a patient-centric approach to integrate the patient's voice into pharmacovigilance deliverables.

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来源期刊
Therapeutic innovation & regulatory science
Therapeutic innovation & regulatory science MEDICAL INFORMATICS-PHARMACOLOGY & PHARMACY
CiteScore
3.40
自引率
13.30%
发文量
127
期刊介绍: Therapeutic Innovation & Regulatory Science (TIRS) is the official scientific journal of DIA that strives to advance medical product discovery, development, regulation, and use through the publication of peer-reviewed original and review articles, commentaries, and letters to the editor across the spectrum of converting biomedical science into practical solutions to advance human health. The focus areas of the journal are as follows: Biostatistics Clinical Trials Product Development and Innovation Global Perspectives Policy Regulatory Science Product Safety Special Populations
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