GERPAC Consensus Conference – Guidance on the Assignment of Microbiological Shelf-life for Hospital Pharmacy Aseptic Preparations

S. Crauste-Manciet, I. Krämer, F. Lagarce, V. Sautou, A. Beaney, Julian Smith, V’Iain Fenton-May, J. Hecq, F. Sadeghipour, P. L. Brun
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引用次数: 11

Abstract

Abstract All dosage forms prepared in hospital pharmacies should be labelled with an appropriate shelf-life. This shelf-life should be validated taking chemical, physical and microbiological data into consideration. This guidance focuses on parenteral aseptically prepared products, as they are high-risk preparations. The risk is exacerbated by a requirement for longer shelf lives for reasons of economy and efficiency. The scope of this guidance includes individual patient preparations, preparations prepared in series (same type of preparation being repeatedly prepared) and batch preparations prepared from the same initial bulk admixture.
GERPAC共识会议-医院药房无菌制剂微生物货架期分配指南
医院药房配制的所有剂型均应标明适当的保质期。该保质期应考虑化学、物理和微生物数据进行验证。本指南的重点是无菌制剂,因为它们是高风险制剂。由于经济和效率的原因,对更长的保质期的要求加剧了风险。本指南的范围包括单个患者制剂、系列制剂(重复制备同一类型制剂)和由相同初始散装外加剂制备的批量制剂。
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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12 weeks
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