Pharma manufacturing ERP with GMP quality systems — OOS, deviations, CAPA, stability studies and Schedule H/H1/X drug logs, seeded with 260 products across 20 therapeutic categories.
OOS and deviation workflows with CAPA linkage and closure evidence.
ICH Q1A study design, pull schedules and condition tracking.
MSDS, COA, TDS and BMR generated per product.
Calibration schedules and status across the plant.
Schedule H/H1/X registers maintained digitally.
Environmental monitoring and sterile-area QC records.