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Upload PDF files or paste text. Server-side PDF extraction with page-level source traceability.
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Executive summary
30-second view for QA leadership — scores, closure status, key findings
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Readiness & quality scores
Completeness vs. investigation quality — with dimension breakdowns
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Event timeline
Chronological reconstruction with document source references
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Evidence map
Confirmed facts · assumptions · missing evidence · conflicts — source-traced
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Evidence graph
Causal relationship map between deviation factors
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Do not close until
Mandatory resolution items before this investigation can be closed
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RCA workbench
Candidate paths with evidence-based confidence — no final answer, only hypotheses for investigator review
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GMP defensibility review
Would an inspector challenge this? Potential findings with regulatory references
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Similar cases
Historical patterns and repeat event detection
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CAPA options
Options for QA consideration — not recommendations. CAPA selection is a human QA decision.
⚠️ These are options only. The final CAPA design must be determined by a qualified QA professional based on confirmed root cause and risk assessment. Do not implement without QA review.
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Export investigation package
Download for QMS entry, Word editing, stakeholder review, or regulatory submission
⚠️ AI-assisted draft — qualified QA review and approval required before entry into any GMP record.
Word / Text
Numbered .txt
JSON
QMS API / database
Evidence CSV
Facts + gaps table
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Paste into QMS
QMS-ready field mapping — copy directly into your eQMS form fields
Veeva Vault
QMS field structure
MasterControl
CAPA / deviation fields
Generic QMS
Universal field map
Print / PDF
Full package
Full investigation package preview
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