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质量保证部门核查:里塞尔达对环境绩效评估要求中样本处置的处理方法。

QAU verification: Ricerca's approach to EPA requirements for specimen disposition.

作者信息

Mayer D E, Purdue T W, Weiss B J

机构信息

Ricerca, Incorporated, Painesville, Ohio 44077, USA.

出版信息

Qual Assur. 1994 Dec;3(4):373-8.

PMID:7613747
Abstract

The U.S. Environmental Protection Agency (EPA) Federal Insecticide. Fungicide and Rodenticide Act and Toxic Substance Control Act Standards issued in 1989 presented a new task for the Quality Assurance Unit (QAU). Sections .190 and .195 of these Good Laboratory Practice (GLP) Standards require "quality assurance verification" prior to the disposal of certain specimens. These include "specimens from mutagenicity tests, specimens of soil, water, and plants, and wet specimens of blood, urine, feces, and biological fluids." QAU involvement in the specimen disposition process was a new concept. Other GLP Standards required specimen retention only as long as the quality of the preparation afforded evaluation: the QAU was not included in the procedure. The QAU verification step was included by the EPA to ensure that disposal of the prescribed specimens would not compromise the integrity of the study. A procedure to address verification of specimen disposition as required by the EPA GLP Standards has been implemented by Ricerca's QAU. This presentation provides a description of this approach to QAU verification.

摘要

美国环境保护局(EPA)1989年发布的《联邦杀虫剂、杀菌剂和灭鼠剂法案》以及《有毒物质控制法案》标准给质量保证部门(QAU)带来了一项新任务。这些良好实验室规范(GLP)标准的第.190条和第.195条要求在处置某些标本之前进行“质量保证核查”。这些标本包括“致突变性试验的标本、土壤、水和植物标本,以及血液、尿液、粪便和生物体液的湿标本”。QAU参与标本处置过程是一个新概念。其他GLP标准仅要求在制备质量允许评估的期间保留标本:该程序不包括QAU。EPA纳入QAU核查步骤以确保规定标本的处置不会损害研究的完整性。Ricerca的QAU已实施了一项按照EPA GLP标准要求处理标本处置核查的程序。本报告介绍了这种QAU核查方法。

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