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   What You'll Learn

  • Why paperless manufacturing is now essential for regulated industries.

  • How digital MES ensures FDA and ISO compliance with complete audit trails.

  • Practical methods to reduce documentation errors and eliminate redundant reviews.

  • Real case studies showing measurable results in speed, cost, and compliance.

  • How Industry 4.0 and smart factories enable real-time visibility across operations.


    Why It Matters

  • Meet Regulatory Demands: Digital MES ensures 21 CFR Part 11 and GMP readiness.

  • Reduce Risk: Automation and traceability minimize non-conformances and errors.

  • Improve Efficiency: Eliminate manual reviews and accelerate approvals.

  • Lower Costs: Cut document management and recall expenses by up to 75%.

  • Enable Scalability: Establish a repeatable, validated model across global sites.

   What You Can Share with Others 

  • Executive-friendly visual explaining the shift from paper-based to digital manufacturing.

  • Data-backed insights from McKinsey, Oracle, and AIIM on compliance and efficiency.

  • Quick-reference examples from Boston Scientific, Edwards Lifesciences, and Medtronic.

  • A one-slide summary of MES-driven improvements in quality and time-to-market.

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FAQ

Q: What is the digital thread backbone? 
A: A PLM-driven backbone connecting enterprise BOMs and supply-chain data across the lifecycle.   
Q: How long will this take to review? 
A: 2–3 minutes; concise visuals and key takeaways.Q: What is the first implementation step? 
Q: What’s the first step to get value? 
A: Map BOM sources, suppliers, and risk signals into Teamcenter and Supplier Connect.  
Q: Which metrics should we track? 
A: Time-to-market, cost variance, at-risk part count, change latency, and carbon impact.  
Q: What risks are reduced? 
A: Stockouts, single-source exposure, IP leakage, and rework from late design changes.  
Q: Who should own this? 
A: Supply chain, engineering, and IT architecture jointly, with supplier management.