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亚洲核心档案:标准化 CMC 要求,以促进亚洲最佳案例申报。

Asia Core Dossier: Standardizing CMC Requirement to Facilitate Best Case Submissions in Asia.

机构信息

Pfizer Inc, Kuala Lumpur, Malaysia.

Pfizer Inc, Seoul, Korea.

出版信息

Ther Innov Regul Sci. 2024 Mar;58(2):223-233. doi: 10.1007/s43441-023-00600-7. Epub 2024 Jan 9.

Abstract

When the regulatory requirements are converged or harmonized, the country-specific variance of countries is often reduced or omitted, and this facilitates the possibility of preparing a core dossier that caters to multiple countries. When such options of a core dossier are acceptable to multiple countries, the resource required to prepare the dossier and the time taken to prepare it is also reduced, thus eliminating resource constraints in supporting dossier planning and preparation and indirectly facilitating earlier submission in countries. In this paper, the authors have illustrated a process applied to standardize the dossier requirements amongst selected countries in Asia, producing an output of a core dossier that applies to four submission types amongst these countries. The core dossier adopts the International Council for Harmonization-Common Technical Dossier format as a reference. Main focus is the standardization of format and requirements within the Module 3 or Chemistry Manufacturing Controls sections of the dossier, which from the authors' organizational experience usually notes a higher variances and country-specific elements. Development of the dossier standardization process is due to an internal hurdle within the authors' organization, where global resource constraints and prioritizations of dossier preparation and compliance review process needed to be improved to facilitate earlier or near-simultaneously submissions in the majority of the Asia countries. The paper demonstrates an assessment of the dossier components and standardization to assemble a fit-for-purpose core dossier termed 'Asia Core Dossier' (ACD). ACD has been successfully implemented within the authors' organization to reduce country-specific requirements and facilitate earlier (fit for strategy) submissions in the selected Asia countries. The paper also discusses the tangible benefits of the authors' experiences from utilizing the ACD. Regulatory professionals in different organizations could reference the ACD as a template for preparing a simplified and efficient dossier and as a relevant component of Good Submission Practice (GSubP).

摘要

当监管要求趋同或协调时,各国的特有差异往往会减少或省略,这使得准备一份迎合多个国家的核心档案成为可能。当多个国家可以接受核心档案的这种选择时,准备档案所需的资源和时间也会减少,从而消除了支持档案规划和准备的资源限制,并间接地促进了各国更早提交。本文作者说明了一种应用于亚洲选定国家的档案要求标准化的过程,产生了适用于这些国家四种提交类型的核心档案。该核心档案采用了国际协调理事会-通用技术档案格式作为参考。重点是档案模块 3 或化学制造控制部分的格式和要求的标准化,从作者的组织经验来看,这部分通常具有更高的差异和国家特有元素。该档案标准化过程的开发是由于作者组织内部的一个障碍,即需要改进全球资源限制和档案准备和合规审查过程的优先级,以促进亚洲大多数国家的早期或近乎同时提交。本文展示了对档案组件的评估和标准化,以组装一个适合目的的核心档案,称为“亚洲核心档案”(ACD)。ACD 已在作者组织内成功实施,以减少国家特有要求并促进选定亚洲国家的早期(适合战略)提交。本文还讨论了作者利用 ACD 的经验所带来的有形收益。不同组织的监管专业人员可以将 ACD 作为准备简化高效档案的模板,并将其作为良好提交实践(GSubP)的相关组成部分。

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