Collaborative Real-World Evidence Among Regulators: Lessons and Perspectives.

IF 6.3 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Clinical Pharmacology & Therapeutics Pub Date : 2025-02-01 Epub Date: 2024-10-21 DOI:10.1002/cpt.3457
Andrew E Beck, Melissa Kampman, Cindy Huynh, Craig Simon, Kelly Plueschke, Catherine Cohet, Patrice Verpillat, Kelly Robinson, Peter Arlett
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引用次数: 0

Abstract

The International Coalition of Medicines Regulatory Authorities (ICMRA), comprising 38 global medicines regulatory authorities, collaborates on shared challenges, notably during the COVID-19 pandemic. This article focuses on the ICMRA COVID-19 Real-World Evidence (RWE) and Observational Studies Working Group. The Working Group aimed to address challenges related to RWE and observational studies during the pandemic, resulting in impactful studies and ICMRA statements on international collaboration for RWE and COVID-19 vaccine safety. Reflecting on 3 years of collaboration, the Working Group surveyed members for insights, and recommendations were formulated to enhance research preparedness, collaboration, and response to future public health emergencies. The lessons learned highlight the importance of global collaborations, governance structures for rapid decision-making, and effective utilization of existing networks. Recommendations include the establishment of an international governance structure, a "coalition of the willing" for swift research collaboration, dedicated sub-groups, periodic workshops, common protocols, joint timelines, and data model templates, leveraging existing infrastructure, and strengthening outreach for transparency and engagement. The Working Group envisions repurposing into an RWE strategic and operational entity, contributing to global public health emergency response mechanisms. In conclusion, the Working Group's success lies in effective communication, collaborative research, and leveraging existing infrastructure, with ongoing contributions to global emergency response mechanisms.

监管者之间的合作实证:经验与展望。
由全球 38 个药品监管机构组成的国际药品监管机构联盟 (ICMRA) 就共同面临的挑战开展合作,尤其是在 COVID-19 大流行期间。本文重点介绍 ICMRA COVID-19 真实世界证据 (RWE) 和观察研究工作组。该工作组旨在应对大流行期间与 RWE 和观察研究相关的挑战,开展了具有影响力的研究,并发表了 ICMRA 关于 RWE 和 COVID-19 疫苗安全性国际合作的声明。在对 3 年的合作进行反思后,工作组对成员进行了调查,以了解他们的见解,并提出了加强研究准备、合作和应对未来公共卫生突发事件的建议。这些经验教训强调了全球合作、快速决策治理结构和有效利用现有网络的重要性。建议包括建立国际管理结构、迅速开展研究合作的 "意愿联盟"、专门的分组、定期研讨会、共同协议、联合时间表和数据模型模板、利用现有基础设施以及加强外联以提高透明度和参与度。工作组设想将其调整为一个 RWE 战略和业务实体,为全球公共卫生应急机制做出贡献。总之,工作组的成功在于有效沟通、合作研究和利用现有基础设施,并不断为全球应急机制做出贡献。
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
12.70
自引率
7.50%
发文量
290
审稿时长
2 months
期刊介绍: Clinical Pharmacology & Therapeutics (CPT) is the authoritative cross-disciplinary journal in experimental and clinical medicine devoted to publishing advances in the nature, action, efficacy, and evaluation of therapeutics. CPT welcomes original Articles in the emerging areas of translational, predictive and personalized medicine; new therapeutic modalities including gene and cell therapies; pharmacogenomics, proteomics and metabolomics; bioinformation and applied systems biology complementing areas of pharmacokinetics and pharmacodynamics, human investigation and clinical trials, pharmacovigilence, pharmacoepidemiology, pharmacometrics, and population pharmacology.
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