HVAC System & Clean Rooms
In a pharmaceutical manufacturing environment, area conditions impact the product being manufactured. A poor HVAC System can be a potential source of contamination. GMP regulations require a quality approach to manufacturing to minimize or eliminate contamination. HVAC systems are crucial to pharmaceutical manufacturing because they control the manufacturing environment. A deeper understanding of HVAC and environmental control is essential to ensure the quality product.
A good HVAC design involves determination of key parameters like temperature, humidity, differential pressure between clean rooms, filtration, air flow and classification of clean rooms. It also involves selection of material/equipment & finishes, positioning of process equipment & HVAC accessories within processing area and flow of personal and material.
Basic expectation of HVAC system in pharmaceutical manufacturing facility is to control airborne particles and micro-organisms and maintain temperature, humidity and room pressure.
Green Leap is proficient in designing of Clean Rooms to support linear process flow & efficient operation. Green Leap designs HVAC systems & Clean Rooms considering ease of operation, efficiency, maintenance & compliance. It emphasizes on optimized space utilization through efficient design & effective integration.
We design not only large HVAC systems for plants but also for R&D centres, Warehouses, corporate offices and smaller offices using VRF.
We follow ASHRAE / SMACNA / EU GMP / ISO 14644 standards and provide following services.