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沙特食品药品监督管理局对智能 GxP 检查的监管经验的思考。

Reflections on the Saudi FDA Regulatory Experience with Smart GxP Inspections.

机构信息

Saudi Food and Drug Authority Riyadh, Riyadh, Saudi Arabia.

出版信息

Ther Innov Regul Sci. 2024 Jul;58(4):730-745. doi: 10.1007/s43441-024-00647-0. Epub 2024 Apr 10.

Abstract

Smart GxP inspections have gained increasing attention due to the COVID-19 pandemic, which, understandably, made it challenging for regulatory authorities to conduct on-site inspections. Smart GxP inspections are an oversight approach developed by the SFDA to enable remote compliance assessments of establishments. In this type of inspection, appropriate technical methods and tools (such as livestreaming video) are used without requiring the presence of inspectors onsite, ensuring efficient utilization of resources and the efficiency of inspection process. The objective of this research is to examine and document the shared encounters involving remote inspections and evaluations carried out by SFDA from 2020 to 2022. This will be achieved through the evaluation of the accuracy of document evaluation and the extent to which the objectives of smart GxP inspections were met. Data were collected from local and international smart inspections reports conducted by SFDA between 2020 and 2022, covering medical device manufacturers, pharmaceutical manufacturing sites, warehouses, accreditation offices, scientific offices, and food manufacturing facilities. The results indicate that smart GxP inspections were effective in achieving visit objectives, showing a high degree of document evaluation accuracy. The findings of this study support the use of smart GxP inspections as a valuable alternative to on-site inspections, offering a practical solution to regulatory compliance during the pandemic and beyond. Although the SFDA recognizes the usefulness of smart inspections in upholding regulatory oversight in the face of various challenges, it does not endorse the complete replacement of conventional on-site inspection methods. The SFDA acknowledges significant limitations associated with the current technological resources used in remote regulatory assessments, and these limitations will be explored in the relevant sections.

摘要

由于 COVID-19 大流行,智能 GxP 检查受到了越来越多的关注,这使得监管机构难以进行现场检查。智能 GxP 检查是 SFDA 开发的一种监督方法,可实现对机构的远程合规评估。在这种检查中,使用了适当的技术方法和工具(如直播视频),而无需检查员亲临现场,从而确保了资源的有效利用和检查过程的效率。本研究的目的是检查和记录 2020 年至 2022 年期间 SFDA 进行的远程检查和评估的共同经验。这将通过评估文件评估的准确性以及智能 GxP 检查目标的实现程度来实现。数据来自 2020 年至 2022 年间 SFDA 进行的本地和国际智能检查报告,涵盖医疗器械制造商、制药生产场所、仓库、认证办公室、科学办公室和食品生产设施。结果表明,智能 GxP 检查有效地实现了访问目标,显示出高度的文件评估准确性。这项研究的结果支持将智能 GxP 检查作为现场检查的替代方法,为大流行期间及以后的监管合规提供了实用的解决方案。尽管 SFDA 认识到智能检查在面对各种挑战时对维护监管监督的有用性,但它并不赞成完全取代传统的现场检查方法。SFDA 认识到远程监管评估中使用的当前技术资源存在重大限制,并且将在相关部分探讨这些限制。

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