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
2024-12-01 → 2024-12-10
Actual
2026-08-28 → 2024-01-16
Exceptions
1
Release Risk
medium
Step Timeline
StepStatusStartEndResult
Materials Consumed and Genealogy
LotMaterialStatusGenealogy
LOT-012310Active Pharmaceutical Ingredient A Variant 7expiredOpen workbench
LOT-012311Active Pharmaceutical Ingredient B Variant 7consumedOpen workbench
LOT-012312Active Pharmaceutical Ingredient C Variant 7in-processOpen workbench
LOT-012313Microcrystalline Cellulose Variant 7approvedOpen workbench
LOT-012314Lactose Monohydrate Variant 7approvedOpen workbench
LOT-012315Hydroxypropyl Methylcellulose Variant 7approvedOpen workbench
Equipment and Calibration
AssetStatusCalibration DueQualification
AST-01170 Visual Inspection System #171operational2025-02-18qualified
AST-01171 Weighing Balance #172in-calibration2025-05-11qualified
In-Process Controls and Pending Tests
ControlMeasuredSpecStatus
Exceptions and Deviations
ExceptionSeverityStatusDeviation
Environmental Excursionminoropendev-00886
Environmental ExcursionminoropenNot linked
Environmental ExcursionminoropenNot linked
Environmental ExcursionminoropenNot linked
Environmental ExcursionminoropenNot linked
Environmental ExcursionminoropenNot 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.