Meaningful & Measurable Risk Assessment Tools for Environmental Monitoring Site Selection Program.

Q3 Medicine
Vanessa Vasadi Figueroa
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引用次数: 0

Abstract

The role of Environmental Monitoring has evolved alongside the manufacturing processes and filling technologies its aims to monitor, and so should the risk assessment tools we implement for establishing this important program. Sample site selection, appropriateness of sampling methods, sampling volumes and sampling frequencies are all important components of contamination control for a facility and must be evaluated as appropriate using a robust risk assessment. The types of environmental monitoring required for a robust program will vary based on the type of operation, frequency in which that operation is performed, and the level of risk associated to the process. Learn how to develop a meaningful risk assessment and include measurable risk rankings for 6 applicable categories in biopharmaceutical manufacturing. The process for scoring each of the 6 categories, systematic evaluation of contamination probability and example outcomes will be shared for theoretical EM sites mapped throughout an ISO 5 and 7 cleanroom area, thus ensuring adequate criteria and fair assessment are applied in each case. The methodology for this risk assessment tool will be demonstrated as suitable for environmental monitoring programs during initial site qualification, when evaluating EMPQ results, or when periodically updating the requirements for monitoring during routine operations.

环境监测选址方案中有意义和可测量的风险评估工具。
环境监测的作用随着其监测目标的制造过程和灌装技术的发展而发展,我们为建立这一重要项目而实施的风险评估工具也应如此。采样地点的选择、采样方法的适当性、采样量和采样频率都是设施污染控制的重要组成部分,必须酌情使用可靠的风险评估进行评估。一个健全的程序所需的环境监测类型将根据操作的类型、执行操作的频率以及与该过程相关的风险等级而有所不同。学习如何开发一个有意义的风险评估,并包括可衡量的风险排名在生物制药生产的6个适用类别。对6个类别中的每一个进行评分的过程、污染概率的系统评估和示例结果将在整个ISO 5和7级洁净室区域的理论EM站点中共享,从而确保在每种情况下应用充分的标准和公平的评估。此风险评估工具的方法将被证明适用于环境监测项目的初始场地鉴定,评估EMPQ结果,或在日常操作中定期更新监测要求。
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
1.90
自引率
0.00%
发文量
34
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