Railes MES: See. Control. Optimize. All in one platform
Railes MES allows you to monitor your production in real time, manage processes, optimize operations with AI, and automate the entire manufacturing workflow.
Made to simplify production and increase performance
It is a Manufacturing Execution System (MES) created to integrate and automate activities in production environments, from the factory floor to decision-making managers.
Compliance and Traceability
Ensure full traceability and compliance with industry standards through automated data tracking and reporting.
Quality Management and Control
Maintain high quality standards with real-time monitoring and automated quality control processes.
Customization and Flexibility
Customization options, ensuring seamless integration with existing systems and adaptation to diverse manufacturing processes.
Advanced Data Analytics and Artificial Intelligence
Leverage the power of AI to gain deep insights into your production data and predict future trends.
Your Industry solutions
From Insight to Improvement. Built on 4 Pillars
Visibility
See everything happening on the shop floor in real time, from work orders, machines, operators, downtimes, and performance. A live control panel for your entire operation.
Execution
Digitize production processes. Clear instructions, error-free data entry, full traceability, and standardized operations, all executed directly by the shop floor teams.
Quality
Control and record quality at every step. Inline inspections, nonconformities, and action plans, with complete traceability by lot, operator, and equipment.
Improvement
Turn data into decisions. Analyze root causes of downtime, compare shifts, identify losses, with automated reports and dashboards that power continuous improvement.
Read our blog
Manufacturing Execution SystemMES Integration Guide: Connecting to ERP, SCADA, and IoT
Every minute your shop floor data sits trapped in a silo, you are flying blind. This guide explains exactly how MES connects to ERP, SCADA, and IoT systems, which data flows, which protocols to use, and how to plan an integration project that does not derail your operations.
Quality ManagementHow to Implement a CAPA Process
Most CAPA systems fail not because companies lack a process, but because they treat it as a documentation exercise. This guide presents a 7-step technical approach to CAPA that truly eliminates root causes and meets ISO 9001, ISO 13485, FDA 21 CFR Part 820, and EU GMP requirements.
PharmaceuticalsReview by Exception: How MES Transforms Pharmaceutical Batch Release
A 150-page batch record reduced to a three-page exception report. Batch release cycles compressed from weeks to days. Discover how Review by Exception, powered by MES, transforms pharmaceutical quality assurance.
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Railes MES can enhance efficiency
Discover how our solution can boost your operations.