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  • Audit readiness: SMART-MES makes you ever ready for audit
  • Achieve paperless manufacturing operation and superior productivity
  • Complete Data Capture with Data Integrity
  • Consistent Master and Batch Records generation
  • Material dispensing with FEFO and FIFO
  • Timely Plant maintenance and calibrations
  • Quality deviations are handling automatically
  • Analytical Reports and Trend Analysis
  • Quick access to all relevant batch information

competitive If a Pharma Manufacturing organization fails a regulatory audit, it has to shut the operations, review the quality systems and regulatory compliance system. It has to address all the issues and then invite for re-audit. This results into a loss of minimum six months of revenue. This results into severe loss. The ROI of SMART MES is calculated from that fact that it prevents the Pharma Manufacturing units from failing a regulatory audit.

  • Warehouse Management
    • Raw material warehouse
    • Intermediate product warehouse
    • Finished goods warehouse
  • Work ordering
  • Master Batch Records
  • Material dispensing
  • Formulation Manufacturing
  • Production batch records
  • Deviation management
  • Packaging Work ordering
  • Formulation Packaging
  • Cleaning management
  • Quality Assurance
  • Quality Control
  • Document Management
  • Plant Maintenance
  • Audit readiness: MES makes you ever ready for audit
  • Achieve paperless manufacturing operation
  • Helps you achieve superior productivity
  • Does a complete Data Capture with Data Integrity
  • Master and Batch Records are consistently generated as part of the operations
  • Material dispensing takes care of FEFO and FIFO
  • Plant maintenance and calibrations takes care of timely maintenance/ calibrations
  • Quality deviations are handled automatically


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