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医疗器械的两级过程验证方法

Two-level process validation approach for medical devices.

作者信息

Chen Yeong-Lin

机构信息

a Validation Department , SHL Group , Taoyuan , Taiwan.

出版信息

J Med Eng Technol. 2019 Feb;43(2):139-149. doi: 10.1080/03091902.2019.1626505. Epub 2019 Jun 18.

Abstract

Medical device industry encompasses a wide range of technologies and applications. Due to the diversity, medical device process validation guidance does not suggest a particular strategy and approach of validation implementation as that of pharmaceutical industry. Based on medical device manufacturing characteristics, and philosophies/principles of medical device/pharmaceutical industry process validation guidance documents, this article illustrates two-level process validation approach which includes component production level and device assembly level. In addition, case study is provided to facilitate the understanding of how to utilise the process validation approach.

摘要

医疗设备行业涵盖了广泛的技术和应用。由于其多样性,医疗设备工艺验证指南不像制药行业那样建议特定的验证实施策略和方法。基于医疗设备制造特点以及医疗设备/制药行业工艺验证指南文件的理念/原则,本文阐述了两级工艺验证方法,包括部件生产级和设备组装级。此外,还提供了案例研究以促进对如何运用该工艺验证方法的理解。

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