对沙特 FDA 监管部门智能 GxP 检查经验的思考

IF 2 4区 医学 Q4 MEDICAL INFORMATICS
Ali M. Alhomaidan, Nawaf G. Al-Murikhi, Morae A. Al-Qarni, Fahad A. Al Fahaadi, Khalid S. Al Otaibi, Radwan Hafiz, Ohoud A. Almadani, Turki A. Al Rafie, Mohammed A. Al Ageel, Mohammed A. Dahhas
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引用次数: 0

摘要

智能 GxP 检查因 COVID-19 大流行而受到越来越多的关注,可以理解的是,这给监管当局进行现场检查带来了挑战。智能 GxP 检查是国家食品药品监督管理局开发的一种监督方法,可对企业进行远程合规性评估。在这类检查中,使用适当的技术方法和工具(如视频直播),不需要检查人员亲临现场,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国家食品药品监督管理局在 2020 年至 2022 年期间开展的涉及远程检查和评估的共同遭遇。这将通过评估文件评估的准确性和智能 GxP 检查目标的实现程度来实现。数据收集自国家食品药品监督管理局在 2020 年至 2022 年期间开展的本地和国际智能检查报告,涵盖医疗器械制造商、药品生产基地、仓库、认证办公室、科研办公室和食品生产设施。结果表明,智能 GxP 检查能有效实现检查目标,文件评估准确度高。这项研究的结果支持使用智能 GxP 检查作为现场检查的一种有价值的替代方法,为大流行期间及以后的监管合规提供了一种实用的解决方案。尽管国家食品药品监督管理局认识到智能检查在面对各种挑战时坚持监管的有用性,但并不赞同完全取代传统的现场检查方法。国家食品药品监督管理局承认,目前用于远程监管评估的技术资源存在重大局限性,相关章节将对这些局限性进行探讨。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Reflections on the Saudi FDA Regulatory Experience with Smart GxP Inspections

Reflections on the Saudi FDA Regulatory Experience with Smart GxP Inspections

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.

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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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