Frequently Asked Questions
Everything you need to know about ParaTech Pharma ERP — implementation, modules, compliance, support, hosting, customization and the demo process.
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.
Explore the modules, compliance and implementation in more detail.
Still have questions?
Our local team is happy to walk you through ParaTech Pharma ERP on your own real-world scenarios.