Discover the Vimachem Pharma MES Platform
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Live demonstration with an expert
// Connect one-on-one
See for yourself the advantages of the fully configurable and modular Pharma 4.0 AI-driven MES platform.
Live demonstration with an expert
// Connect one-on-one
See for yourself the advantages of the fully configurable and modular Pharma 4.0 AI-driven MES platform.
OUR FOUR MODULES CAN BE DEPLOYED AS STANDALONE AND FEATURE END-TO-END FUNCTIONALITY ACROSS MANUFACTURING AND QUALITY OPERATIONS.
This allows you to select the software components you need and focus on digitalizing your production step by step.
Pharma MES Platform MODULES
ELECTRONIC BATCH RECORDS (EBR)
A cloud-based digital solution that will help you streamline your production, reduce quality defects and ensure compliance & auditability. Built exclusively for Pharma & Biopharma manufacturers, the software enables faster and more robust implementations.
WEIGH & DISPENSE MODULE (WDM)
A digital solution that enables you to streamline your dispensing activities and ensure compliance & efficiency. Built for Pharma & Biopharma manufacturers, the software is pre-validated & built on modern technology, enabling faster and more robust implementations.
MACHINE CONNECTIVITY
Plug-and-Produce universal machine connectivity automatically collects, transforms, and analyzes data at the source, providing critical real-time visibility to avoid downtime and production losses.
MANUFACTURING ANALYTICS
Multi-tenant cloud platform enables instant manufacturing analytics and insights from anywhere, including OEE machine performance and production monitoring, reporting via APIs, and enterprise tools (ERP, LIMS, APS) integrations.
TRACEABILITY
A cutting-edge traceability software platform, designed in collaboration with Tracelink, allows integration to any Level 2 and corporate Level 4 system, enabling compliance with global traceability standards while optimizing serialization and aggregation operations.
DIGITAL LOGBOOKS
Digitize paper-based logbooks and forms and enable recording and integration of data from equipment, machines, processes, and operators to increase process visibility and comply with cGMP and FDA 21 CFR 211.182.
