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Get the free Good Laboratory Practice (GLP) - Compliance Monitoring Programme. GLP Manual

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Wilton Park House, Wilton Place, Dublin 2, Ireland Tel +353 1 607 3003 Fax +353 1 607 3109 Email IAB.i.e. Web www.inab.ie Good Laboratory Practice (GLP) Compliance Monitoring Program GLP Manual Issue
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Good Laboratory Practice (GLP) is a quality system framework governing the planned and controlled laboratory activities, ensuring the generation of reliable and consistent laboratory data for regulatory purposes.
Any laboratory involved in non-clinical health and environmental safety studies, particularly those conducting experiments or tests on substances for regulatory purposes, are required to follow and file Good Laboratory Practice (GLP) reports.
Filling out Good Laboratory Practice (GLP) requires compliance with the specific guidelines set forth by the regulatory agency overseeing the study. Generally, it involves documenting all study objectives, methodologies, procedures, results, and conclusions in a comprehensive manner, ensuring accuracy and traceability of data.
The purpose of Good Laboratory Practice (GLP) is to promote and ensure the quality, reliability, and integrity of laboratory data generated during non-clinical safety testing of chemicals, drugs, and other substances. It serves as an internationally recognized standard for testing facilities, enhancing the credibility and acceptability of study results.
Good Laboratory Practice (GLP) reports should include precise descriptions of the study objectives, methods, test items, test systems, analytical methods, results, individual observations, and conclusions drawn from the data. It should also provide information on the quality control procedures, equipment used, standard operating procedures, and personnel involved in the study.
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