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Pharma MES Platform

Pharma MES Platform

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Pharma MES Platform

  • Overview
  • Key features
  • Benefits
  • Industry

Overview

Vimachem’s Pharma MES Platform is a modular, AI-driven system built specifically for pharmaceutical and biotech companies. It streamlines production, ensures regulatory compliance, and enables real-time monitoring of processes and equipment. With advanced analytics, paperless operations, and machine integration, it empowers manufacturers to transform digitally with confidence. Whether you're digitizing batch records or optimizing warehouse traceability, Vimachem adapts to your workflows and scales as you grow.

Pharma MES Platform

Key Features

Electronic Batch Records (EBR):

Automates batch documentation, ensures GMP compliance, and provides full traceability—eliminating paper-based errors and accelerating production review.

Weigh & Dispense Module (WDM):

Improves accuracy and efficiency during raw material handling with guided workflows and real-time checks, reducing manual entry errors.

Machine Connectivity (IIoT Enabled):

Connects shop floor machines to the MES, enabling real-time performance tracking, predictive maintenance, and centralized data visibility.

Serialization Site Management (SSM):

Tracks and manages serialization and aggregation, ensuring compliance with DSCSA, EU FMD, and other global traceability regulations.

Smart Warehouse Traceability (SWT):

Monitors materials across storage and production zones, ensuring lot-wise tracking, FIFO enforcement, and seamless inventory reconciliation.

Benefits

Regulatory Compliance

Meets global GMP and 21 CFR Part 11 standards with audit-ready documentation and traceability.

Faster Production Cycles

Reduces batch review times, minimizes downtime, and enables quicker lot release through digital workflows.

Scalable Implementation

Flexible architecture allows phased rollouts—start small, expand globally without disrupting existing systems.

Industry

Pharmaceuticals

Pharmaceuticals

FAQs

Yes, it is 21 CFR Part 11 and EU Annex 11 compliant, designed specifically for regulated life sciences manufacturing.

Absolutely. Vimachem supports seamless integration with popular ERP, LIMS, SCADA, and PLC systems via APIs.

Timelines vary, but most clients begin with a pilot module and scale within 6–12 months.

The platform supports all pharma modalities—biologics, injectables, solids, and even personalized medicine manufacturing.

Yes, Vimachem provides both global on-site implementation and 24/7 remote support.