GMP-compliant precision weighing for pharmaceutical operations
Privya Solution's Pharma Weighing System delivers fully GMP-compliant dispensing, sampling, and bulk weighing operations with complete electronic batch records, 21 CFR Part 11 audit trails, and multi-balance integration.
Direct RS232/USB/Ethernet integration with analytical, precision, and floor-scale weighing balances across the facility.
Step-by-step dispensing workflow with mandatory tare, pre-weigh, and post-weigh verification at every stage.
Complete eBMR with automatic capture of weights, operator, date/time, and balance calibration status.
Full electronic signature support, audit trail, user access control, and data integrity compliance.
Theoretical vs actual batch quantity comparison with automatic alerts on variance exceeding defined limits.
GMP-compliant dispensing labels with lot, quantity, operator, date, and unique dispensing ID.
QC sampling workflows with sample identification, storage location tracking, and LIMS integration.
Balance calibration schedule management with blocking of uncalibrated instruments and certificate storage.
Shift-wise dispensing summary, variance reports, compliance dashboards, and regulatory-ready PDFs.
Production order received from planning system. System creates dispensing request with BOM, standards, and allowed variance.
Operator scans material barcode, system verifies expiry, quarantine status, and quantity availability.
Balance connected in real-time. Tare value automatically captured. Weighing starts with live display.
Weight captured directly from balance. System checks against target range and alerts on deviation.
Complete eBMR auto-generated with weights, operator ID, e-signature, timestamps, and balance calibration status.
Batch quantity verified, deviations logged, and batch released to next stage only after supervisor e-sign approval.
Reduced material variance from 2.1% to 0.3% across batches
Eliminated manual errors — 100% electronic batch record compliance
Cut sample preparation time by 45% with automated recording
Passed FDA audit with zero data integrity observations
Reduced batch dispensing cycle by 30%
Achieved Schedule M compliance in 3 weeks post-implementation
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