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Home Manual Details
Author:
WAHO
Category:
Quality Control Laboratories
Language:
English
Date Updated:
8/11/2020 6:32:53 PM
Description
To clearly define the consistent steps to be taken in the identification, investigation, evaluation and documentation of out of specification test results to ensure validity of analytical data.
Abstract
1.0 Purpose: To clearly define the consistent steps to be taken in the identification, investigation, evaluation and documentation of out of specification test results to ensure validity of analytical data. 2.0 Scope: This procedure applies to all OOS Physico-chemical analytical result generated within the laboratory. This procedure does not apply to microbiology. 3.0 Responsibility: The Analyst and Head of Unit should carry out all investigations on OOS analytical results in strict compliance with the requirement set out in this SOP. The Quality Assurance Manager should ensure that the provisions of this SOP are complied with. The head of laboratory is responsible for the overall monitoring and coordination of the OOS investigations for the laboratory.
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