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   What You'll Learn   

  • Core vs. Context and why MES is “context” 
  • Regulated-industry drivers: FDA 21 CFR Part 11, ISO 13485  
  • Outsourcing models for Siemens Opcenter MES  
  • Compliance-ready operations with proactive monitoring and updates  
  • Cost and scalability benefits vs. in-house management  
  • Real-world proof points from leading manufacturers  

    Why It Matters

  • Refocused R&D and product innovation time  
  • Audit readiness sustained by specialist governance  
  • Lower downtime risk and faster incident response  
  • Reduced internal overhead and skills bottlenecks  
  • Measurable outcomes: uptime, MTTR, audit findings 

   What You Can Share with Others    

  • Core vs. Context one-page explainer 
  • MES outsourcing ROI and risk summary 
  • Partner evaluation checklist for regulated MES 
  • SLA criteria list for uptime and response 
 

 

Download the executive brief

See how expert-run MES protects compliance while your teams build what differentiates.

FAQ

Q:Why classify MES as “context,” not “core”? 
A: It’s essential for compliance and efficiency but doesn’t differentiate your business.  

Q: Which regulations does this support? 
A: FDA 21 CFR Part 11 and ISO 13485, among others for life sciences and devices.  

Q: What platforms are covered? 
A: Siemens Opcenter MES, with lifecycle management and updates.  

Q: What benefits do peers see? 
A: Examples note outsourced IT, supply chain, and manufacturing to protect core innovation.  

Q: Why Connected Manufacturing™ Technology? 
A: Siemens Expert Partner with regulated-industry expertise and proactive support.