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
2025-11-20 → 2025-12-01
Actual
2025-02-09 → 2024-12-17
Exceptions
11
Release Risk
high
Step Timeline
StepStatusStartEndResult
Materials Consumed and Genealogy
LotMaterialStatusGenealogy
LOT-010598Sodium Hydroxide Variant 9holdOpen workbench
LOT-010599Phosphoric Acid Variant 9rejectedOpen workbench
LOT-010600Active Pharmaceutical Ingredient AexpiredOpen workbench
LOT-010601Active Pharmaceutical Ingredient BconsumedOpen workbench
LOT-010602Active Pharmaceutical Ingredient Cin-processOpen workbench
LOT-010603Microcrystalline CelluloseapprovedOpen workbench
LOT-010604Lactose MonohydrateapprovedOpen workbench
Equipment and Calibration
AssetStatusCalibration DueQualification
AST-01228 Incubator #229in-maintenance2026-01-18requalification-due
AST-01229 Autoclave Sterilizer #230out-of-service2026-02-04not-qualified
In-Process Controls and Pending Tests
ControlMeasuredSpecStatus
Exceptions and Deviations
ExceptionSeverityStatusDeviation
Late Stepminorcloseddev-00515
Late StepminorclosedNot linked
Late Stepminorcloseddev-01015
Late Stepminorcloseddev-00515
Late StepminorclosedNot linked
Late StepminorclosedNot 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.