QA / QC Management

Batch release that doesn't wait on manual cross-checks

Unify QC test results, specification limits, deviation records, and CAPA threads against the active electronic batch record. Make quality disposition decisions on connected live data, not re-typed spreadsheet numbers.

Batch release that doesn't wait on manual cross-checks

Automated specification verification

Test results entered against a batch are evaluated against approved specification limits instantly, flagging out-of-specification points the moment they are logged.

Instant Certificate of Analysis (COA) generation

Generate compliant CoAs automatically from verified, signed-off QC data without manually re-entering values into separate document templates.

Closed-loop OOS to CAPA tracking

Out-of-specification or out-of-trend results immediately open linked investigation threads, tying root-cause analysis and corrective actions directly to the triggering batch.

4-HourStreamlined batch release cycles
AutomaticSpecification limit evaluation
Zero-LeakageQuarantine interlocks until QA sign-off
Closed-LoopOOS/OOT to CAPA enforcement

Built to handle the messy reality of pharma operations

Batch records, sensor telemetry, quality interlocks, and compliance infrastructure built for modern life science plants.

01

Real-time QC integration with electronic batch records

Laboratory test results link directly to the manufacturing batch and raw material lots. If any parameter falls outside approved limits, SICORG automatically enforces a quarantine hold, preventing unreleased stock from moving downstream.

  • Direct specification limit matching for raw materials, in-process controls, and finished goods
  • Automated material quarantine interlocks triggered upon OOS detection
  • Secure electronic signature sign-offs for final QA product disposition
Real-time QC integration with electronic batch records
02

Connected investigations and deviation workflows

Manage deviations, change controls, and corrective/preventive actions in a single seamless thread. Every investigation retains full traceability to the affected batch, equipment, and analyst.

  • Investigation records auto-linked to triggering batches and test records
  • CAPA tracking with mandatory root-cause analysis and effectiveness checks
  • Comprehensive quality history accessible for permanent batch archives
Connected investigations and deviation workflows

Make every pharma operation more connected

One AI-native ERP for production, quality, inventory, finance, and compliance.