ERP Software for Pharmaceutical Manufacturing in India
We build custom pharmaceutical ERP where the audit trail matters as much as the throughput. Batch manufacturing records, validated processes, lot genealogy and expiry control, with the documentation discipline regulated production demands — designed so an inspection is a report, not a fire drill.
( What you get )
Built for Pharma
Formulation & BMR
Master formulations and batch manufacturing records with electronic sign-off at each stage.
QA / QC workflows
In-process checks, release testing, quarantine and disposition controlled by role.
Lot genealogy & expiry
Full genealogy from API through to finished pack, with expiry-driven stock control.
Compliance & audit trail
Tamper-evident audit logging and validation documentation aligned to your regulator.
Serialisation & despatch
Serialisation and track-and-trace support for the markets that mandate it.
( FAQ )
Questions, answered
Can you build to GMP and validation requirements? add
We design for GMP-aligned operation — controlled electronic records, role-based sign-off, tamper-evident audit trails — and produce the validation documentation your quality team needs. Formal validation is executed with your QA function, since it certifies your process, not our code.
Does it handle serialisation and track-and-trace? add
Yes, where your markets mandate it. Serialisation, aggregation and reporting are built to the specific regulatory scheme rather than a generic implementation.
Can it integrate with our lab and QC instruments? add
We integrate LIMS and instrument outputs where they expose interfaces, so results attach to the batch record automatically instead of being transcribed.
ERP Development for other industries
( Next step )
Need ERP Software for Pharmaceutical Manufacturing?
Let's scope your project. We reply within 24 hours.