用于评估化学制药公司生产中的合规性和成本的管理工具

F. Rank, W. Steven, H. Scheuermann, T. Wozniewski, R. Müller
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引用次数: 1

摘要

由于严格和日益苛刻的良好生产规范(GMP)和客户要求,化学制药行业的公司都面临着评估和衡量合规性和成本的巨大挑战。在先灵股份公司内部确定了对生产实施符合性测量工具的需要,并开展了相关活动。建立的合规性评价体系和第一个合规性成本体系模型结构良好,适用于生产。因此,该系统可以被其他领域和化学制药公司采用,甚至可以扩展到其他领域,例如良好实验室规范(GLP)和良好临床规范(GCP)。版权所有©2005 John Wiley & Sons, Ltd
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Management tools for the evaluation of compliance and costs in the production of chemical–pharmaceutical companies
Due to the stringent and increasingly demanding Good Manufacturing Practice (GMP) and customer requirements, companies within the chemical–pharmaceutical sector share the enormous challenge of evaluating and measuring compliance and costs. The need for implementing a compliance measuring tool for production was identified within the Schering AG and activities were undertaken. The established compliance evaluation system and the first model for a compliance cost system proved to be well-structured and suitable for the production. Consequently, the systems can be adapted by other areas and chemical–pharmaceutical companies and may even be expanded to other areas, such as Good Laboratory Practice (GLP) and Good Clinical Practice (GCP). Copyright © 2005 John Wiley & Sons, Ltd.
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