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
2025-12-30 → 2026-01-03
Actual
2026-10-06 → 2025-01-06
Exceptions
1
Release Risk
low
Step Timeline
StepStatusStartEndResult
Materials Consumed and Genealogy
LotMaterialStatusGenealogy
LOT-011290Active Pharmaceutical Ingredient A Variant 3quarantineOpen workbench
LOT-011291Active Pharmaceutical Ingredient B Variant 3holdOpen workbench
LOT-011292Active Pharmaceutical Ingredient C Variant 3rejectedOpen workbench
LOT-011293Microcrystalline Cellulose Variant 3expiredOpen workbench
LOT-011294Lactose Monohydrate Variant 3consumedOpen workbench
Equipment and Calibration
AssetStatusCalibration DueQualification
AST-01174 Karl Fischer Titrator #175cleaning-required2025-12-31not-qualified
AST-01175 Dissolution Tester #176operational2024-11-26qualified
AST-01176 Hardness Tester #177operational2025-02-14qualified
In-Process Controls and Pending Tests
ControlMeasuredSpecStatus
Exceptions and Deviations
ExceptionSeverityStatusDeviation
Late StepminorclosedNot linked
Late StepminorclosedNot linked
Late Stepminorcloseddev-01359
Late Stepminorcloseddev-00859
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.