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
2026-04-08 → 2026-04-11
Actual
2026-08-18 → In progress
Exceptions
18
Release Risk
medium
Step Timeline
StepStatusStartEndResult
Materials Consumed and Genealogy
LotMaterialStatusGenealogy
LOT-010927Hydrochloric Acid 37%approvedOpen workbench
LOT-010928Sodium HydroxideapprovedOpen workbench
LOT-010929Phosphoric AcidapprovedOpen workbench
LOT-010930Active Pharmaceutical Ingredient A Variant 1quarantineOpen workbench
LOT-010931Active Pharmaceutical Ingredient B Variant 1holdOpen workbench
LOT-010932Active Pharmaceutical Ingredient C Variant 1rejectedOpen workbench
LOT-010933Microcrystalline Cellulose Variant 1expiredOpen workbench
Equipment and Calibration
AssetStatusCalibration DueQualification
AST-01322 Film Coater #323operational2025-04-11qualified
AST-01323 Capsule Filler #324operational2025-10-01requalification-due
In-Process Controls and Pending Tests
ControlMeasuredSpecStatus
Exceptions and Deviations
ExceptionSeverityStatusDeviation
Missing Signaturemajorunder-reviewNot linked
Missing Signaturemajorunder-reviewdev-00062
Missing Signaturemajorunder-reviewNot linked
Missing Signaturemajorunder-reviewdev-00562
Missing Signaturemajorunder-reviewdev-00062
Missing Signaturemajorunder-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.