Batch manufacturing ERP for chemicals and pharma
Batch-accurate production with a complete, audit-ready record of every batch, from raw material receipt to the customer.
Built for every part of chemicals & pharma.
Your problems, named. And what we build for each.
Every batch needs a full record of weights, readings, signatures, deviations and yield
Master formula and an electronic batch production record for every batch
Materials must not be used before QC releases them
Quarantine and release status on every lot, blocked until approved
Regulators expect a full audit trail and controlled signatures
Audit log of who changed what, when and why; signatures for release and deviations
Expired or near-expiry stock gets used or sold
Expiry on every lot, first-expiry-first-out issue and expiry alerts
Recalls must find every affected customer fast
Forward and backward lot traceability from supplier lot to customer shipment
Deviations and corrective actions tracked on paper
Deviation and corrective action workflow linked to the batch
One connected process, from first order to final payment.
Every step below is a screen in your system, and every step updates the next automatically.
- Raw material receipt
- Quarantine
- QC test & release
- Dispensing to master formula
- Batch production
- Finished batch QC
- QA release
- Packing with batch & expiry
- Dispatch
- Complaints & recall
Go further when you're ready.
Machine data, live.
Reactor and dryer temperature and pressure monitoring, environmental monitoring of clean areas and energy per batch.
Explore Smart Factory →AI that pays back.
Document AI for certificates of analysis, demand forecasting by formulation and a knowledge assistant for SOPs.
Explore Eletva AI →Choose how to start.
Start where it hurts most. Every package runs on the same platform, so you can grow without starting over.
Inventory with batch and expiry, purchase, sales, GST billing
Adds formulas, batch production, QC and QA release, traceability and documents
Adds electronic batch records, deviations and corrective actions, validation support, multi-plant
Questions we hear often.
Is the system ready for regulated pharma production?
It supports batch records, audit trails, signatures and QA release. Formal computer system validation is scoped separately for each client's regulations.
Can we stop unreleased material from being used?
Yes. Every lot carries a quarantine or release status, and unreleased lots cannot be issued to production.
Do you handle expiry dates?
Yes. Expiry is tracked on every lot, stock is issued first-expiry-first-out, and near-expiry lots trigger alerts.
Let's talk about your chemicals & pharma business.
Tell us what slows you down. We'll show you what to fix first and how fast it can be live.