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Screenshots

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Details

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MESvantage Main Features

• Fast Setup
  The SaaS can be live on your factory floor in about 90 days.
• Real-Time Data
  It turns your machine and system data into live, useful information.
• Silos and Security
  Each customer has their own secure, separate environment, which keeps data safe and private.
• Validated Platform
  The SaaS is certified and tested to meet medical manufacturing standards like ISO 13485 and 21 CFR Part 11.
• Connects All Systems
  It can link your ERP, quality system, machines, and metrology tools in one place.
• Business Intelligence
  Uses dashboards and reports, like Power BI, for managers and executives to see key data.
• Purpose-Built for CDMOs
  All workflows are designed specifically for contract manufacturing in medical device companies.
• Regulatory Documentation
  Generates required validation documents like IQ, OQ, and PQ reports.
• Quality and Compliance Tools
  Includes features for inspections, non-conformance reports, corrective actions, and validation evidence.
• Complete Manufacturing Records
  It creates detailed device history records and traces all manufacturing steps.
• Dedicated Customer Environment
  Each customer’s data is kept separate and secure, making validation easier.
• Customer Portals and Digital Tools
  Offers portals for OEM customers, digital signage, and mobile apps for operators.
• Designed for Medical Manufacturing
  It is built specifically for regulated medical device contract manufacturers.
• Performance and Efficiency Insights
  Provides data on equipment efficiency and downtime, helping to improve production.

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MESvantage Alternatives

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Technologies Used

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