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
2025-05-09 → 2025-05-16
Actual
2025-01-16 → In progress
Exceptions
1
Release Risk
low
Step Timeline
StepStatusStartEndResult
Materials Consumed and Genealogy
LotMaterialStatusGenealogy
LOT-011710Active Pharmaceutical Ingredient A Variant 7approvedOpen workbench
LOT-011711Active Pharmaceutical Ingredient B Variant 7approvedOpen workbench
LOT-011712Active Pharmaceutical Ingredient C Variant 7approvedOpen workbench
Equipment and Calibration
AssetStatusCalibration DueQualification
AST-01220 Laminar Flow Cabinet #221in-calibration2026-04-02qualified
AST-01221 Isolator #222in-maintenance2025-09-02qualified
AST-01222 WFI Still #223out-of-service2026-05-11qualified
AST-01223 RO System #224cleaning-required2025-07-31requalification-due
AST-01224 Compressed Air System #225operational2025-04-20not-qualified
AST-01225 HVAC Unit #226operational2025-09-20qualified
In-Process Controls and Pending Tests
ControlMeasuredSpecStatus
Exceptions and Deviations
ExceptionSeverityStatusDeviation
Late StepcriticalopenNot linked
Late StepcriticalopenNot linked
Late StepcriticalopenNot linked
Late StepcriticalopenNot linked
Late StepcriticalopenNot linked
Late StepcriticalopenNot 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.