Validation Ready
Compliance Built-in
Batch Recall
Tailored workflows built for your unique industrial attributes and constraints.
Accelerate throughput with real-time WIP monitoring and bottleneck detection.
Hyper-localized tax engines and global trade standards built into the core.
High-fidelity executive dashboards for 100% supply chain transparency.
Seamlessly integrates with your industrial business ecosystem:
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High-security recipe protection with bill-of-material scaling based on active ingredient purity.
Pre-built workflows for clinical documentation, hygiene logs, and mandatory pharma audits.
Integrated digital signatures, audit trails, and strict user access logs for US FDA compliance.
Instantaneous 2nd-level drill-down from raw material lot to final retail box for rapid recall.
Automated scheduling and recording of material stability tests as per international data standards.
Integrated project tracking for new formulation development and clinical trial documentation.
Integrated Lab Information Mgmt for automated Certificate of Analysis (COA) generation.
Real-time visibility into active ingredient loss during complex pharmaceutical reactions.
FEFO (First-Expiry-First-Out) logic for sensitive raw materials and finished medicines.
Comprehensive Field-Force automation (SFA) to monitor Medical Representative performance.
Pharmaceutical excellence is built on data integrity. RexoERP provides a resilient, unalterable digital core that ensures every batch meets the highest medical standards.
Built-in safeguards against recipe errors and incompatible lot mixing.
Effortlessly scale production across multiple factory units and new drug markets.
RexoERP integrates advanced machine learning and autonomous logic to transform static data into high-fidelity strategic intelligence.
AI models that analyze environmental and POTANCY data to optimize batch output.
Real-time monitoring of FDA/GMP standards with predictive risk alerts.
Dynamic formulation adjustments using AI to ensure consistent product potency.