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• Even small temperature or humidity deviations in pharmaceutical and medical products can lead to high costs and reputational risk.
• A simple “real-time alarm” is not sufficient; the duration, frequency, and product impact of deviations must be evaluated together.
• If moments such as shipment, transfer, and waiting are not measured, processes become invisible and quality management remains reactive.
• End-to-end lifecycle view: Each product or batch is evaluated within a single history, including all locations, durations, and exposure conditions.
• Less noise, clearer prioritization: Not every deviation has the same impact. Plasmon+ provides decision-support outputs such as “no intervention required.”
• Transparent and traceable reporting: Enables fast and consistent access to historical data for audits and internal controls.
• Even minor temperature or humidity deviations in pharmaceutical and medical products can result in high costs and reputational risk.
• A simple “real-time alarm” is not sufficient; the duration, frequency, and impact on the product must be evaluated together.
• If moments such as shipment, transfer, and waiting are not measured, processes become invisible and quality management remains reactive.
GMP / GDP-Compliant Warehouses and Pharmaceutical Warehouses
Vaccine Storage Areas and Stability Testing Rooms
Hospital, Clinic, and Pharmacy Cabinets
Blood and Organ Banks (Environmental Condition Traceability)
• İlaç üreticileri ve dağıtıcıları
• Ecza depoları ve sağlık lojistiği sağlayıcıları
• Hastane ve klinik kalite / biyomedikal ekipleri
• Denetim süreçlerini dijital ve şeffaf yönetmek isteyen kurumlar