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.
Open Batches
6
Updated 2h agoReleased Qty
12,420
Updated 2h agoYield %
98.7%
Updated 2h agoBuilt To Solve Pharma Challenges.
Replace spreadsheets, manual batch records, and siloed systems with a single traceable, auditable platform.
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 Configure plants, units and formula access controls.
- 2 Import BOMs, historical batches and suppliers.
- 3 Run MRP, schedule production and prepare QC tests.
- 4 Release batches upon QC approval and push to distribution.
- 5 Close inventory, accounting entries and generate compliance reports.
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.
