The pharmaceutical industry operates in production environments shaped by strict regulations and high hygiene standards. ProManage MES digitalizes production processes even in hygienic zones, making physically restricted areas fully visible and manageable.

It establishes a digital bridge between production, planning, and method engineering units, enabling end-to-end uninterrupted monitoring of operations. As a result, planning teams can monitor production in real time and respond quickly to any disruptions.

• With station-based downtime tracking and detailed stoppage reporting, all efficiency-reducing factors on the production line become visible. This enables planned maintenance, shorter response times, and measurable improvement in Overall Equipment Effectiveness (OEE).
• Fully compatible with primary–secondary production structures, ProManage MES can monitor two separate lines (primary and secondary) simultaneously with a single Smart Counter IoT device. This eliminates the need to purchase separate hardware for each line, reduces additional device costs, and ensures a more efficient investment.
• Provides a digital documentation infrastructure compliant with regulations such as GMP; product traceability, quality test processes, and operator competency management (polivalence) are centrally monitored to minimize error rates.
• Also supports the implementation of TPM, Lean Manufacturing, and World Class Manufacturing (WCM) methodologies to enhance productivity, reduce costs, and facilitate regulatory compliance.

With ProManage, transparency, quality assurance, and regulatory compliance in pharmaceutical production come together in a single platform – while also optimizing your investment costs.