Friedli D, Kappeler W, Zimmermann S
Spirig AG, Froschacker, Egerkingen, Switerzerland. szimmerm@cilch. jnj.com
Pharm Acta Helv. 1998 Feb;72(6):343-8. doi: 10.1016/s0031-6865(97)00032-0.
In recent years the introduction of computer systems for data handling in the pharmaceutical industry has increased. A standard LIMS (laboratory information management system) is software commercially available from different suppliers not only to facilitate data handling in laboratories but also to cover GMP-requirements. Computer systems introduced in GMP-areas of pharmaceutical companies have to be validated. For a standard LIMS, the general validation of the program is performed by the supplier. Nevertheless, the user is always required to cover all phases of a validation. The objective of this paper is to discuss suitable test procedures for the most critical functions of a standard LIMS needed during the verification step of the validation process.
近年来,制药行业中用于数据处理的计算机系统的引入有所增加。标准的实验室信息管理系统(LIMS)是一种可从不同供应商处商业购买的软件,不仅用于方便实验室的数据处理,还能满足GMP要求。引入制药公司GMP区域的计算机系统必须经过验证。对于标准的LIMS,程序的一般验证由供应商进行。然而,用户始终需要涵盖验证的所有阶段。本文的目的是讨论在验证过程的验证步骤中所需的标准LIMS最关键功能的合适测试程序。