Built for Pharmaceutical Manufacturers

VERIXOR — Modern ERP for 
Pharma Manufacturing

From formula control and batch traceability to QA workflows and regulatory reporting, VERIXOR centralises your operations so you can produce safer, compliant medicines at scale.

Trusted by manufacturers & distributors
Reduce batch release time by up to 30%
Production snapshot
VERIXOR Plant — Unit 4
GMP-compliant

Open Batches

6

Updated 2h ago

Released Qty

12,420

Updated 2h ago

Yield %

98.7%

Updated 2h ago
Inventory health
Raw materials value ₹ 2.1 Cr
Batch traceability Expiry alerts QC hold lists

Built To Solve Pharma Challenges.

Replace spreadsheets, manual batch records, and siloed systems with a single traceable, auditable platform.

Lack of batch traceability
Manual QC & release processes
Complex formulation and version control
Inventory expiry & recalls risk
Disconnected finance & production data

Batch & Formula Management

Versioned formulations, controlled access, and precise batch calculations.

Quality & Compliance

QC workflows, hold/release, SOP mapping and audit-ready documentation.

Inventory & Warehouse

Batch-wise stock, expiry alerts, barcode scanning and multi-location control.

Production Planning

MRP, scheduling, capacity planning and shop-floor integration.

Sales & Distribution

Batch-wise invoicing, expiry-aware dispatch and distributor management.

Finance & Regulatory Reporting

Integrated ledger, tax, cost of goods, and compliance reports for audits.

Modular. Configurable. Pharma-centric.

Deploy only what you need — combine Production, QA, Inventory, Sales and Finance modules into a single ERP tailored to your plants and compliance needs.

  1. 1 Configure plants, units and formula access controls.
  2. 2 Import BOMs, historical batches and suppliers.
  3. 3 Run MRP, schedule production and prepare QC tests.
  4. 4 Release batches upon QC approval and push to distribution.
  5. 5 Close inventory, accounting entries and generate compliance reports.
GMP & regulatory templates Multi-plant & multi-currency ready

QC Automation

Auto-trigger tests

Define test plans per material and auto-hold batches that fail.

Audit Trails

Full traceability

Immutable logs for batch changes, QC, and approvals.

SOP & Docs

Linked to batches

Attach SOPs, certificates and COAs to production runs.

Recall Support

Rapid recalls

Find affected lots and follow recall workflows with minimal downtime.

Ready To Modernise Your Pharma Operations?

Request a personalised walkthrough — we’ll show production, QA, and inventory flows configured for your plant.

Frequently Asked Questions

BatchMaster ERP is a process-manufacturing ERP tailored for pharmaceutical manufacturers to manage formulation/R&D, batch production, quality, traceability, compliance, planning, warehousing, and costing in a single system while adhering to FDA/cGMP and 21 CFR Part 11 requirements.

It supports cGMP processes, electronic records/signatures (21 CFR Part 11), audit readiness, CAPA, non-conformance, SOP control, BMR/MBR, COA generation, supplier management, and bi-directional lot traceability to meet FDA/GxP expectations.

Yes. The solution tracks non-conformance, manages CAPA workflows, logs quality transactions, and supports quality/stability testing within batch processes.

Features include secure formula management with versioning, patenting, pre-defined templates for capsules, softgels, etc., label claims, comparison, approvals, batch scaling/resizing, physical property management, and formula BOMs for packaged/batch entries.

Yes—tracks lots/expiry, manages FEFO, supports quarantine/holds, and enforces SOPs and quality checks across receiving, production, and dispatch with complete audit trails, as well as controls lot movements based on quality statuses.

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