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
2025-07-28 → 2025-08-07
Actual
2025-12-10 → 2025-04-06
Exceptions
17
Release Risk
critical
Step Timeline
StepStatusStartEndResult
Materials Consumed and Genealogy
LotMaterialStatusGenealogy
LOT-012037Hydrochloric Acid 37% Variant 7quarantineOpen workbench
LOT-012038Sodium Hydroxide Variant 7holdOpen workbench
LOT-012039Phosphoric Acid Variant 7rejectedOpen workbench
LOT-012040Active Pharmaceutical Ingredient A Variant 8expiredOpen workbench
LOT-012041Active Pharmaceutical Ingredient B Variant 8consumedOpen workbench
LOT-012042Active Pharmaceutical Ingredient C Variant 8in-processOpen workbench
LOT-012043Microcrystalline Cellulose Variant 8approvedOpen workbench
LOT-012044Lactose Monohydrate Variant 8approvedOpen workbench
LOT-012045Hydroxypropyl Methylcellulose Variant 8approvedOpen workbench
Equipment and Calibration
AssetStatusCalibration DueQualification
AST-01279 Torque Tester #280cleaning-required2025-11-04not-qualified
AST-01280 Granulator #281operational2025-07-18qualified
AST-01281 Tablet Press #282operational2025-12-22qualified
In-Process Controls and Pending Tests
ControlMeasuredSpecStatus
Exceptions and Deviations
ExceptionSeverityStatusDeviation
Environmental ExcursionmajorclosedNot linked
Environmental ExcursionmajorclosedNot linked
Environmental ExcursionmajorclosedNot linked
Environmental ExcursionmajorclosedNot linked
Environmental ExcursionmajorclosedNot linked
Environmental ExcursionmajorclosedNot 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.