End-to-End MES Solutions, Strategic Consulting & System Integration for Pharmaceutical Excellence
We combine advanced technology with deep industry experience to streamline processes, drive growth, and reduce costs. Our collaborative approach ensures fast, efficient project delivery with minimal risk.
Partner with experts who understand pharmaceutical excellence
We are committed to providing the most effective MES and integration solutions to meet the specific needs of pharmaceutical clients. Click on any service to learn more.
End-to-end Manufacturing Execution System deployment for pharmaceutical excellence.
View Details →Strategic Generic Master Batch Record design to streamline manufacturing.
View Details →Seamless integration of MES with enterprise systems.
View Details →Transform manufacturing data into actionable insights.
View Details →End-to-end serialization and track-and-trace solutions.
View Details →Expert guidance for regulatory compliance and transformation.
View Details →End-to-end Manufacturing Execution System deployment covering every stage of the production cycle, from biotech API manufacturing to packaging and quality operations.
"Our MES solutions cater to every stage of the production cycle, including biotech API manufacturing, formulation, fill and finish, packaging, and quality operations. We deliver tailored services to ensure product quality, traceability, compliance, and overall operational excellence.
From initial assessment through go-live and optimization, we guide you through every phase with deep pharmaceutical expertise and proven methodologies.
Reduce batch release time by 40-60%
Achieve end-to-end product traceability
Ensure full GxP compliance
Improve manufacturing quality
Implementation timelines typically range from 6-18 months depending on system complexity, scope, and organizational readiness. We develop a detailed project schedule during the assessment phase.
We design implementation to minimize production disruption through phased rollouts, parallel systems running, and careful go-live planning.
We ensure full compliance with FDA 21 CFR Part 11 for electronic records and signatures, EU GMP requirements, and GAMP 5 guidelines for system validation.
Let's discuss your MES requirements and create a customized implementation plan.
Get MES Implementation ConsultationStrategic Generic Master Batch Record design that reduces complexity, accelerates time-to-market, and improves compliance.
"Our GMBR design services help you consolidate and optimize your master batch record portfolio. Using proven parameter-based design principles, we reduce the number of distinct MBRs required while maintaining the flexibility to support product variations and process changes.
This reduces documentation workload, improves compliance, and accelerates technology transfers.
Dramatically reduce your MBR count
Accelerate technology transfers
Decrease documentation time
Improve manufacturing flexibility
Industry-standard pharmaceutical manufacturing execution system trusted by top global pharmaceutical companies.
"PAS-X is the industry standard for pharmaceutical manufacturing execution. As certified implementation partners, we leverage proven methodologies, pre-configured templates, and deep PAS-X expertise to deliver rapid, low-risk implementations.
More than half of the world's top 30 pharmaceutical companies trust PAS-X for their critical manufacturing operations.
Break down IT/OT silos with comprehensive integration services connecting MES with enterprise systems.
"We specialize in connecting your MES with ERP, LIMS, DCS, PLC, SCADA, and other enterprise systems. Our integration solutions enable real-time data flow, complete traceability, and Industry 4.0 capabilities.
SAP, Oracle, JDE for material management and planning
Complete quality data integration and COA generation
Real-time process data and equipment integration
Unified monitoring and control
Transform raw manufacturing data into actionable insights for continuous improvement.
"Our advanced analytics solutions provide real-time production monitoring, predictive maintenance capabilities, and comprehensive business intelligence. We design and implement data warehouses, analytics platforms, and dashboards that give you visibility into every aspect of your manufacturing operations.
Live production dashboards and alerts
Machine learning for maintenance optimization
Root cause analysis and trend detection
Executive dashboards and reporting
End-to-end serialization and product traceability solutions that meet global regulatory requirements.
"We deliver end-to-end serialization and traceability solutions with precision and excellence. Our expertise spans barcode implementation, GS1 compliance, anti-counterfeiting measures, and digital track-and-trace technologies.
Expert guidance for regulatory compliance and strategic digital transformation.
"We provide comprehensive GxP compliance and strategic consulting services, helping pharmaceutical companies achieve high standards of quality and compliance. Our consultants bring deep expertise in FDA 21 CFR Part 11, EU GMP, GAMP 5, and other regulatory frameworks.
Electronic records and signatures compliance
Computerized systems validation
Risk-based validation approach
Computer system validation lifecycle
Installation, operational, performance qualification
Regulatory inspection readiness
Empower your team with MES expertise and operational excellence skills.
"We provide comprehensive training and capability building programs to empower your team with MES expertise. Our training covers everything from basic system navigation to advanced optimization techniques, customized to match your operations.
System navigation and daily operations
Advanced features and troubleshooting
System configuration and maintenance
Strategic system utilization and KPIs
Regulatory requirements and best practices
Build internal training capabilities
Transforming Pharmaceutical Manufacturing Through Technology and Expertise
Founded with a mission to help pharmaceutical manufacturers optimize their operations through advanced MES solutions and strategic consulting, AutoMESys Manufacturing Solutions brings together decades of collective experience in manufacturing execution systems, regulatory compliance, and digital transformation. Our team of industry experts is dedicated to partnering with pharmaceutical and biotech companies to achieve operational excellence and sustainable growth.
To empower pharmaceutical and biotech manufacturers with transformative MES solutions and expert consulting that drive operational excellence, ensure regulatory compliance, and enable sustainable growth.
A pharmaceutical manufacturing industry where advanced systems, data-driven insights, and expert partnership enable manufacturers to deliver quality products efficiently while maintaining the highest standards of compliance and excellence.
We deliver nothing but the best. Quality is embedded in everything we do, from our solutions to our service delivery.
We embrace emerging technologies and methodologies to solve complex manufacturing challenges and drive continuous improvement.
We work collaboratively with our clients, understanding their unique challenges and co-creating solutions that align with their business goals.
We bring deep, specialized knowledge in pharmaceutical manufacturing, GxP compliance, and MES systems to every engagement.
Our team comprises seasoned manufacturing professionals, system architects, regulatory consultants, and change management experts. Our consultants bring extensive experience from leading pharmaceutical companies, contract manufacturers, and system integrators. With specializations spanning biotech, small molecules, advanced therapies, and CDMO operations, our team possesses the breadth and depth needed to tackle complex implementation challenges.
Stay informed with the latest insights, whitepapers, case studies, and best practices in pharmaceutical manufacturing.
In-depth technical papers on MES implementation, validation, and optimization strategies.
View Whitepapers →Real-world success stories from pharmaceutical manufacturers worldwide.
Read Case Studies →Practical guides for implementing and optimizing MES in pharmaceutical manufacturing.
Download Guides →On-demand webinars covering topics from GMBR design to advanced analytics.
Watch Webinars →Annual reports and trend analysis for pharmaceutical manufacturing technology.
View Reports →Regular updates on MES trends, regulatory changes, and technology innovations.
Read Blog →We'd love to hear from you. Get in touch and let's discuss how we can help you achieve manufacturing excellence.