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Frequently asked questions
Yes. The same pharmaceutical-grade controls — batch records, QA/QC, FEFO and traceability — apply to veterinary pharma, nutraceutical and contract manufacturing operations.
ParaTech Pharma ERP is built around DRAP and WHO-GMP readiness with electronic BMR, CoA, stability studies and locked audit trails, plus FBR Digital Invoicing and POS compliance.
Most clients go live in 8–14 weeks following our structured methodology: discovery, master data, configuration, training, parallel run, go-live and post-go-live support.
Yes. Contract and toll manufacturing is built in — with isolated cost centers, independent batch numbering, customer-owned materials and client-branded CoAs alongside your own brands.
Support is provided by our Lahore-based engineering team, both remote and on-site — reachable, accountable and responsive.