GLP Audit Report Template | Good Laboratory Practice FDA 21 CFR 58 | Editable Word PDF | Lab Compliance Internal Audit

GLP audits require structured, evidence-based reporting of SOP compliance, data integrity, equipment calibration, study conduct, and QA oversight—because inspection readiness depends on how clearly compliance is verified and documented. This GLP Audit Report Format helps you streamline the audit process by capturing audit scope, observations, nonconformities, and CAPA in one professional report—so your audit reporting stays consistent, complete, and inspection-ready.

This is a ready-to-use, professionally designed, and fully customizable audit report created to streamline your audit process. It supports internal audits, facility audits, study audits, and regulatory readiness by providing a standardized structure aligned with GLP expectations. Everything is organized to help auditors document checks faster, reduce reporting gaps, and improve closure of findings through clear corrective action tracking.

Whether you audit laboratories, QA units, archives, computerized systems, analytical operations, or study documentation, this format supports stronger GLP documentation, smoother management review, and better readiness for inspections.

What’s Included:

• Audit cover page and report header (facility/study, audit type, date, auditor details)
• Audit scope, objectives, criteria, and GLP reference section
• Facility/study overview and audit plan summary (customizable)
• Findings and evidence recording fields (area-wise / process-wise)
• SOP and documentation review section (controlled docs, records, deviations)
• Equipment calibration, maintenance, and qualification verification section
• Data integrity and raw data review summary fields (customizable)
• QA program and audit trail verification section (as applicable)
• Nonconformity/observation log with classification fields (customizable)
• CAPA section (root cause, corrective action, owner, target date, verification)
• Closing meeting summary, audit conclusion, management sign-off, follow-up timeline

Key Benefits:

• Streamlines GLP audit reporting with a standardized, ready-to-use format
• Improves inspection readiness with consistent evidence and data integrity documentation
• Reduces reporting time with structured sections for findings and CAPA
• Supports faster corrective action closure with clear ownership and due dates
• Strengthens compliance tracking for SOPs, calibration, records, and QA oversight
• Improves audit trail quality for regulators, sponsors, and management review
• Fully customizable for facility audits, study audits, and vendor audits
• Ideal for GLP laboratories, test facilities, CROs, and QA teams

Get your GLP Audit Report audit report format today and streamline your audit process.