About this view

This batch detail page ties execution evidence, material genealogy, equipment fitness, in-process controls, and quality events into one release-focused view. Users can trace each unit operation against timestamps and investigate linked exceptions without leaving context. The panelized layout supports QA review by exception while preserving full evidence access. Next actions include closing residual issues and completing disposition-ready evidence checks.

Planned
2026-09-08 → 2026-09-21
Actual
2024-03-11 → 2026-01-20
Exceptions
4
Release Risk
medium
Step Timeline
StepStatusStartEndResult
Materials Consumed and Genealogy
LotMaterialStatusGenealogy
LOT-011230Active Pharmaceutical Ingredient A Variant 1expiredOpen workbench
LOT-011231Active Pharmaceutical Ingredient B Variant 1consumedOpen workbench
LOT-011232Active Pharmaceutical Ingredient C Variant 1in-processOpen workbench
LOT-011233Microcrystalline Cellulose Variant 1approvedOpen workbench
LOT-011234Lactose Monohydrate Variant 1approvedOpen workbench
LOT-011235Hydroxypropyl Methylcellulose Variant 1approvedOpen workbench
Equipment and Calibration
AssetStatusCalibration DueQualification
AST-01210 Visual Inspection System #211operational2025-07-06qualified
AST-01211 Weighing Balance #212operational2025-04-26qualified
In-Process Controls and Pending Tests
ControlMeasuredSpecStatus
Exceptions and Deviations
ExceptionSeverityStatusDeviation
Missing SignatureminoropenNot linked
Missing SignatureminoropenNot linked
Missing Signatureminoropendev-01206
Missing Signatureminoropendev-00706
Missing SignatureminoropenNot linked
Missing SignatureminoropenNot linked
QA Review Checklist and Signatures
  • Step execution completeness verified with signed evidence.
  • All high-severity exceptions dispositioned or justified.
  • QC release tests reviewed and OOS investigations closed or dispositioned.
  • Final release signatory validated with segregation-of-duties check.
No release readiness record found.