SYSPRO enables pharmaceutical manufacturers to maintain stringent regulatory compliance, track raw materials and finished goods by batch, and ensure consistent quality control throughout the production lifecycle.
From formulation to packaging, SYSPRO helps streamline operations, reduce risk, and respond to regulatory demands with speed and accuracy.
Pharmaceutical manufacturing requires complete traceability, real-time quality checks, and strict documentation. SYSPRO delivers centralized control over inventory, recipes, batch production, and audits—supporting compliance with FDA, cGMP, and other global standards.
With integrated planning, costing, and document control, SYSPRO enables rapid, compliant scaling across multiple product lines.
Track ingredients, intermediates, and final products by batch for full compliance and recall readiness.
Align with FDA 21 CFR Part 11, cGMP, and GAMP standards with built-in audit trails and digital approvals.
Manage approved formulations and automatically adjust for batch scaling with precision and control.
Enforce approval workflows and secure documentation with audit-ready digital signatures.
Isolate inventory pending quality checks or regulatory approval to prevent release of non-compliant goods.
Monitor lot aging, expiry dates, and re-testing schedules to ensure timely distribution and regulatory adherence.
Configure SYSPRO to match your unique manufacturing processes, regulatory requirements, and operational workflows. Our industry-agnostic approach ensures optimal system performance regardless of your production environment or business model.
With built-in tools for traceability, documentation, and regulatory compliance, SYSPRO supports pharmaceutical manufacturers in delivering safe, effective products while navigating strict industry standards with confidence.
Try SYSPRO for your business
