Discover the Vimachem Pharma MES Platform
Manufacturing Analytics & OEE
Manufacturing Analytics & OEE
AI-driven Manufacturing Analytics and Data Management solution for pharma and biotech manufacturers that increases efficiency and throughput while reducing production costs.
// MA & OEE
Product Tour
Optimize Performance with Real-Time Insights
Disconnected systems and limited visibility make it difficult for pharma manufacturers to respond quickly to production inefficiencies. Vimachem’s Manufacturing Analytics & OEE module provides real-time insights into critical KPIs - enhancing performance monitoring, equipment utilization, and compliance with GMP and operational excellence standards.
Pharma-Specific OEE Reporting
Implementation delays due to lengthy validation cycles can stall digital transformation and increase costs. Vimachem’s pre-validated solution includes a comprehensive, out-of-the-box validation package -reducing deployment timelines by at least two months while ensuring full compliance from the initial rollout.
Seamless System Integration
Manual data entry and fragmented systems can lead to operational blind spots and increased risk. Vimachem’s MA&OEE module integrates effortlessly with your ERP, shop floor industrial equipment, and RFID systems—providing a unified, real-time view of production performance without the need for additional infrastructure or complex IT setup
// How it Works
See Vimachem’s MA & OEE in Action
// MA & OEE
Built for Pharma and Biotech Teams to Drive Performance, Compliance, and Operational Excellence
Pharmaceutical and biotech manufacturers need to maximize throughput while maintaining quality and meeting regulatory requirements. Vimachem’s Manufacturing Analytics & OEE module provides the insights and tools needed to improve efficiency, standardize operations, and ensure compliance across all production sites.
Vimachem’s Manufacturing Analytics & OEE solution empowers pharma and biotech teams to drive continuous improvement, ensure compliance, and unlock higher productivity, delivering smarter, faster, and more efficient manufacturing across all sites.
This solution provides:
- A GAMP5 Category 4, GMP-compliant platform purpose-built for pharmaceutical and biotech environments.
- Real-time monitoring of performance, downtime, and changeovers to identify and address inefficiencies.
- A user-friendly, intuitive interface with pharma-specific dashboards designed for operators, supervisors, and managers with no coding required.
- Automated alerts that highlight production issues and enable fast, informed responses.
- Seamless integration with ERP systems, machines, and RFID readers to unify data across operations.
With deep expertise in machine and data protocols, Vimachem’s automation and software engineers have completed machine data connectivity projects in over 20 countries worldwide.
Our proven capabilities in machine data acquisition, combined with our deep technical knowledge of the pharmaceutical environment makes us the ideal partner for connecting machines across the pharmaceutical shop floor.
Advance Continuous Improvement with Smart OEE
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Plug-and-Optimize in Days
Begin fully automating OEE calculations in just hours - no invasive setup, no downtime. Real insights and fast results.
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Empower Shop Floor Teams
AI-powered, operator-centric tools streamline shift handovers, instructions, and reporting - driving daily performance gains.
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Data-Driven Decisions
Track KPIs and improvement plans with PDCA-based dashboards that simplify operational excellence initiatives.
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Real-Time Alerts
Minimize unplanned downtime with automated alerts that highlight root causes and guide rapid resolution.
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Pharma Focus
A GAMP5 Category 4, GMP-compliant solution to compare and evaluate manufacturing data across multiple facilities through a single, unified interface.
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Digital Continuous Improvement
Identify, assign and monitor continuous improvement routines and tasks and improve efficiency while reducing costs and employee turnover.
Our journey with Vimachem has been truly rewarding. From connecting machines to installing the Vimachem MES platform, we rapidly integrated 6 packaging lines without any production disruptions.
George Vlassopoulos, Head of Engineering, Elpen
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GxP Features
User Permissions & Security
Role-based access, AD integration, and reduced IT admin effort.
Verified Data Integrity
System validation, input checks, and secure access control.
Electronic Signatures
Fully compliant with FDA 21 CFR Part 11 and EU GMP Annex 11.
Comprehensive Digital Records
Full traceability of shop floor actions and equipment usage.
Audit Logs
Track every system activity for compliance and troubleshooting.
Flexible Data Exports
Export data in XLSX/CSV formats manually or automatically.
Changeover Instruction & Analytics
Guide operators through the changeover process with step-by-step instructions to reduce delays and boost operational efficiency.
Electronic Batch Record
Combine with eBR to streamline packaging records and ensure full compliance.
Serialization Site Manager
Track serialization efficiency and monitor packaging line performance with a single machine connection.
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