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Good laboratory practice information


The Principles of Good Laboratory Practice (GLP) are guidelines for managing non-clinical health and environmental studies effectively.[1] They cover how studies are planned, conducted, recorded, and reported. These principles define roles and responsibilities within test facilities, set standards for facilities and equipment, emphasize the use of standard procedures, and require proper documentation and record-keeping. Overall, GLP ensures studies are conducted responsibly and produce reliable results for regulatory purposes globally.[2]

  1. ^ "OECD Principles of Good Laboratory Practice (as revised in 1997)". OECD Environmental Health and Safety Publications. 1. OECD. 1998. Archived from the original on 20 April 2010. Retrieved 15 October 2006.
  2. ^ "OECD Principles of Good Laboratory Practice (GLP) and GLP Compliance Monitoring". Organisation for Economic Co-operation and Development. Retrieved April 28, 2024.

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bodies to ISO/IEC/17020. Proficiency testing scheme providers Good Laboratory Practice (GLP) test facilities for compliance to OECD GLP principles SANAS...

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Standardisation Information Technology GLP Federal Bureau for Good Laboratory Practice In the scope of the statutory remit of risk assessment in the area...

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Laboratory

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or laboratory, it is necessary to understand the requirements of the standard, evaluation of the current safety, health and environmental practices and...

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tested once and accepted everywhere' can be realised. Accreditation Good laboratory practice (GLP) Institute for Reference Materials and Measurements (IRMM)...

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committees: Good Clinical Practice Committee Good Laboratory Practice Committee Good Manufacturing Practice Committee Good Pharmacovigilance Practice Committee...

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revelations of misconduct by IBT Labs led to the establishment of Good Laboratory Practice standards and regulations for industrial testing. In 1991, Philip...

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