Designed for Regulatory Rigor
In pharma, software bugs aren't just inconvenient; they're critical risks. We deploy audited, validated ERP workflows.
Quality Assurance (QA) & CAPA
Automated quarantine of incoming goods until lab test approval. Integrated Corrective and Preventive Action (CAPA) tracking.
Batch & Expiry Traceability
Full bi-directional traceability. Track any raw material batch forward to the final product, or reverse-track a product to its origin.
Electronic Signatures (21 CFR 11)
Secure, audited approval workflows requiring PINs/Biometrics for critical actions like releasing a batch for sale.
Recipe Management
Strict version control for formulations. Handle active ingredient potencies and automatic yield calculations for process manufacturing.
FEFO Inventory Picking
First Expired, First Out strategy strictly enforced across all warehouses to minimize write-offs due to shelf-life expiration.
Cold Chain Integration
Integrate with IoT temperature sensors during transport to ensure biologicals and vaccines remain within strict thermal thresholds.
Automated Compliance
Regulatory audits can shut down operations if paperwork is missing. Our ERP digitises the entire quality pipeline, ensuring every action is logged, authenticated, and ready for FDA/EMA inspection.
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✓De-risk Audits: Instant retrieval of batch manufacturing records (BMR) and audit trails.
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✓Zero Spoilage: Advanced FEFO rules drastically reduce financial losses from expired raw materials.
Audit Readiness
Every database change is stamped with an immutable timestamp and user ID.
Mock Recall Speed
Trace a defective API batch to all affected customers in a few clicks.
Pharma ERP Questions
Do you assist with CSV (Computer System Validation)?
Yes. We provide standard IQ/OQ/PQ protocols and documentation as part of our implementation methodology to ensure the system is fully validated for regulatory compliance.
Can the ERP integrate directly with our LIMS (Laboratory Information Management System)?
Absolutely. We frequently build API bridges between the ERP and external LIMS so quality test results automatically release quarantined batches without double data entry.
Secure your supply chain
Talk to our life sciences practice leads to see a demo of our validated workflows.
Request a Pharma Demo