Laboratories · Quality Control · Advanced
GLP compliance self-assessment checklist covering organisation, QA, facilities, SOPs, study conduct, and archives.
Good Laboratory Practice (GLP) ensures the quality and integrity of non-clinical safety studies used in regulatory submissions. This compliance checklist covers the key GLP principles: management responsibilities, quality assurance, facilities and equipment, standard operating procedures, test and reference items, study conduct, reporting, and archiving.
Use this checklist for internal GLP readiness assessments or as preparation for regulatory authority inspections. Systematic GLP self-audits identify compliance gaps before they become findings during official inspections.
This checklist template is provided as a general-purpose resource and is not tailored to the regulatory requirements of any specific country, region, or jurisdiction. It is the responsibility of each organisation to review and adapt this template to ensure compliance with all applicable local laws and regulations. Miratag does not accept liability for any inaccuracies or omissions, or for any actions taken based on this template.
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