GIQAR position paper on ‘Archiving and Good Laboratory Practice’†

M. Brunetti, P. Albertini, D. Andreozzi, M. Astolfi, M. Capasso, S. Caroli, E. Corbascio, M. Filippone, E. Invernizzi, R. Lasala, E. Lombardini, G. Malanca, F. Medioli, B. Mónico, Francesco Motta, R. Rizzello, A. Tonnicchi, F. Uberti, R. Valenti, V. Sforza
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Abstract

Archiving of documents and specimens generated during a non-clinical laboratory study is a basic Good Laboratory Practice (GLP) requirement. The records and materials that should be archived as well as the characteristics and the organisation of archive facilities are addressed in the OECD Series on Principles of Good Laboratory Practice No. 1 (OECD Principles of Good Laboratory Practice (as revised in 1997) [1]. However, in recent years, questions concerning archiving have been raised and the need for a more detailed guidance on this matter has become evident The aim of the Society for Applied Pharmacological Sciences/Italian Group of Quality Assurance in Research (SSFA/GIQAR) working group on ‘Archiving according to GLP’ was to issue a position paper, present it for discussion in an ad hoc round table with representatives of the Italian GLP monitoring authority to promote common standards and to provide additional recommendations on storage and retention of records. Copyright © 2005 John Wiley & Sons, Ltd.
GIQAR关于“存档和良好实验室规范”的立场文件†
将非临床实验室研究过程中产生的文件和标本存档是良好实验室规范(GLP)的基本要求。应存档的记录和材料以及存档设施的特征和组织在OECD关于良好实验室规范原则系列第1号(OECD良好实验室规范原则(1997年修订))中有说明[1]。然而,近年来,关于存档的问题已经提出,对这一问题的更详细指导的需求已经变得明显。应用药理学学会/意大利研究质量保证小组(SSFA/GIQAR)关于“根据GLP存档”的工作组的目标是发布一份立场文件,将其提交给意大利GLP监测当局的代表在一个特设圆桌会议上讨论,以促进共同标准,并就记录的储存和保留提出其他建议。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。
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