Life Sciences
Pioneering CFD-driven innovation and efficiency in life sciences environments
Our CFD expertise accelerates commissioning, regulatory acceptance and operational efficiency across the life sciences sector by ensuring compliant temperature-sensitive storage, cleanrooms, laboratories, and healthcare facilities. With Danish Medicines Agency authorized projects, we asses HVAC designs for temperature, humidity, air change, and particle contamination. From concept to commissioning, we optimize environmental performance and energy efficiency, meeting rigorous standards.
Temperature Mapping for Compliance
Danish Medicines Agency authorized CFD methodology that accelerates commissioning by 2-12 months.
Cleanroom Design and Energy Optimization
Achieving particle compliance while improving energy efficiency in controlled environments.
Risk Mitigation
Early CFD simulations indicate whether rooms will meet compliance criteria, allowing design adjustments.
Avoiding Over-dimensioning
Simulations evaluate designs under seasonal variations and worst-case conditions, reducing CAPEX and OPEX.
From concept to commissioning and beyond
Expertise from early conceptual design through detailed review and design qualification to commissioning.
Thermal Management for Device Cooling
CFD simulations enable efficient cooling in sealed medical devices, minimizing dust and contamination risks.
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CFD-driven validation, enhancing compliance and design efficiency
Using CFD simulations, we accurately model life science environments, from climate-controlled warehouses to cleanrooms as well as medical devices. By validating CFD results against physical measurements, we ensure compliance for HVAC performance and environmental controls. Our Danish Medicines Agency authorized methodology has accelerated temperature mapping compliance, delivering actionable insights for safe, compliant, and energy-efficient designs.
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