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Revised USP chapter <841> enables 50% Out-of-Specification reduction

机译:修订后的USP <841>章可将不合格率降低50%

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摘要

The two largest sources of laboratory errors come from sample processing (30%) and human operation (19%). In addition, the amount of laboratory time spent processing samples is estimated to be greater than 60%. The revised USP Chapter <841> Specific Gravity, posted in February 2013, states that samples can now be prepared by weight, as well as by the historical method of volume. Gravimetric liquid dispensing compensates for any under- or overshoot of the sample weight to produce extremely accurate, confirmed concentrations. Stock and final solutions are prepared in fewer steps and with minimal human interaction. Implementing a gravimetric sample preparation system reduces laboratory errors and Out-of-Specification (OOS) incidents by up to 50%, while increasing laboratory efficiency. Download the white paper on gravimetric sample preparation and find out how the revision of USP Chapter <841 > could benefit you. Simply visit: www.mt.com/q-byebyeml.
机译:实验室错误的两个最大来源来自样品处理(30%)和人为操作(19%)。另外,估计处理样品所花费的实验室时间量大于60%。修订后的《美国药典》第<841>章“比重”于2013年2月发布,指出现在可以按重量以及历史体积方法制备样品。重量液体分配可补偿样品重量的任何过低或过高,以产生极其准确的确认浓度。储备液和最终解决方案的制备步骤更少,并且无需人工干预。实施重量分析样品制备系统可将实验室错误和不合格(OOS)事件减少多达50%,同时提高实验室效率。下载有关重量分析样品制备的白皮书,并了解USP <841>章的修订版如何使您受益。只需访问:www.mt.com/q-byebyeml。

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