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Pharma MES (Manufacturing Execution Systems)

Digitally transform your production processes to reduce risk, boost efficiency and ensure regulatory compliance.

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Safeguard Data Integrity and Transparency

Reduce Error, Boost Efficiency

Automate, guide and digitally record procedures according to cGMP guidelines.

Ensure Compliance

Generate electronic batch records and embedded audit trails in compliance with FDA 21 CFR Part 11 and EU Annex 11. 

Track and Trace

Achieve greater product traceability through integrated batch genealogy and visualization.

Fully Integrated Production

MES foundation that seamlessly integrates with all supporting enterprise-wide production functions.

Bring Reliability and Consistency to Pharmaceutical Manufacturing

Market demands, regulatory requirements and aggressive sustainability goals are increasing pressure on pharmaceuticals. Manual documentation processes are no longer practical and a digital transformation to a pharma MES is needed to:

  • Increase production quality

  • Reduce waste, time and cost

  • Respond rapidly and mitigate risk

 

Accelerate your Pharma 4.0 journey today.

"We view our Electronic Batch Record System (eBRS) as an incredible transformation program we are deploying to make our Digital Data & Analytics (DDA) strategy a reality. DDA will enable us to deliver our Pharma Supply Chain Future-Ready Ambition."

— Andrew Jenkins, Manufacturing Platform Director, GSK

 

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