Issue / CAPA Log (OBX319-301)
📚 Part of the OBX-319 Regulatory Dossier — Reader's Guide. This article shows the live document; edits to the source appear here automatically.
This is a mock / simulation document, made for a portfolio and for learning. The drug (GLPI-103), the sponsor, the people, and the data are all fictional. It is not a real regulatory submission and has no clinical, legal, or regulatory standing. What is real is the shape of the thing — the document structure, the standards it follows, and the analysis methods; the content inside is illustrative.
What it is. Issue / CAPA Log (OBX319-301)
Why it exists. A quality record showing how the program controls quality and builds the audit trail.
How it is produced here. It is a quality record: a plan or log that shows how the program controls quality and builds the audit trail sitting behind every other document.
Format & governing standard. —
Issue / CAPA Log (OBX319-301)
Document ID: QA-003
Version: 1.0
Change History: 1.0 — Initial issue.
Standard(s): ICH E6(R3)
Issue / CAPA Log — OBX319-301
Corrective- and preventive-action register for OBX319-301: issue description, root-cause analysis, corrective and preventive actions, owners, due dates, and effectiveness checks. ICH E6(R3) quality management.
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