Who We Are
What Is Pharmaceutical Supply Chain Software?
Pharmaceutical supply chain software is a custom platform for tracking drug batches, managing cold chain logistics, and maintaining the documentation trail required for regulatory audits, designed around your specific manufacturing and distribution setup. Generic supply chain tools are built for speed and volume, which matters in pharma too, but they usually lack the batch traceability, temperature monitoring integration, and audit-ready documentation structure that pharmaceutical operations need by default. It covers batch tracking, cold chain monitoring, serialisation and compliance, distributor management, and pharmacy inventory systems.
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40
+Professional Experts
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100
+Projects Complete
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6
+Years of Experience
Solution Provide
Our Pharma Technology Services
This is where most of our pharmaceutical technology work concentrates:
End-to-end batch tracking from manufacturer to distributor to pharmacy, with a complete audit trail
Explore MoreDocumentation, SOPs, and regulatory reporting built to align with CDSCO and GMP requirements
Explore MoreTemperature and humidity tracking across storage and transit, with automated alerts for excursions
Explore MoreOrder management, inventory tracking, and expiry monitoring for pharmaceutical distribution networks
Explore MoreData collection, patient tracking, and regulatory submission support for clinical operations
Explore MoreFAQ
Frequently Aksked Questions
The specific goals of a marketing agency can vary depending on the client's needs, industry.
1. How much does pharmaceutical supply chain software cost to build?
A focused batch tracking and distributor management system typically starts around ₹7-12 lakhs. A full compliance management system with cold chain integration and serialisation usually costs more, depending on regulatory scope.
2. How long does it take to build a pharma compliance management system?
A basic batch tracking and documentation platform can be built in 10 to 14 weeks. A full compliance system with serialization, cold chain monitoring, and ERP integration typically takes 5 to 8 months.
3. Do your systems support CDSCO and Schedule M compliance requirements?
Yes. Regulatory alignment is built into how we structure batch records, audit trails, and documentation, not added as an afterthought once the core system is built.
4. Is post-launch support available for pharma software?
Yes. We offer ongoing maintenance covering bug fixes, regulatory update alignment, and feature additions, since pharma compliance requirements tend to evolve with each new regulatory revision.