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
2025-11-17 → 2025-11-22
Actual
2025-12-11 → In progress
Exceptions
7
Release Risk
critical
Step Timeline
StepStatusStartEndResult
Materials Consumed and Genealogy
LotMaterialStatusGenealogy
LOT-012999Phosphoric Acid Variant 9approvedOpen workbench
LOT-010000Active Pharmaceutical Ingredient AapprovedOpen workbench
LOT-010001Active Pharmaceutical Ingredient BapprovedOpen workbench
LOT-010002Active Pharmaceutical Ingredient CapprovedOpen workbench
LOT-010003Microcrystalline CellulosequarantineOpen workbench
LOT-010004Lactose MonohydrateholdOpen workbench
LOT-010005Hydroxypropyl MethylcelluloserejectedOpen workbench
Equipment and Calibration
AssetStatusCalibration DueQualification
AST-01114 Shrink Wrapper #115operational2025-02-12not-qualified
AST-01115 Checkweigher #116in-calibration2026-01-11qualified
In-Process Controls and Pending Tests
ControlMeasuredSpecStatus
Exceptions and Deviations
ExceptionSeverityStatusDeviation
Missing Signatureminorunder-reviewNot linked
Missing Signatureminorunder-reviewNot linked
Missing Signatureminorunder-reviewNot linked
Missing Signatureminorunder-reviewNot linked
Missing Signatureminorunder-reviewdev-00358
Missing Signatureminorunder-reviewNot 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.