HVAC DESIGNING

Heating ventilation and air-conditioning system is a significant energy-consuming part of pharmaceutical manufacturing. Over half of info energy is consumed by the HVAC system of the structure. Our accomplished pharma engineers at QUANTUM design the systems to accomplish the most extreme power efficiencies without weakening on cGMP rules.

In a pharmaceutical manufacturing environment, area conditions influence the thing being created. A poor HVAC System can be a normal wellspring of debasement. GMP rules require a quality method for managing manufacturing to restrict or clear out contamination. HVAC systems are vital for pharmaceutical manufacturing since they control the manufacturing environment. A more significant appreciation of HVAC and environmental control is central to ensure the quality thing.

A good HVAC design incorporates assurance of key limits like temperature, sogginess, differential strain between clean rooms, filtration, wind current and classification of clean rooms. It moreover incorporates assurance of material/gear and totally finishes, arranging of collaboration equipment and HVAC extras inside dealing with district and stream of individual and material.

The basic assumption for an HVAC system in a pharmaceutical manufacturing system is to control airborne particles and small-scale natural elements and stay aware of temperature, moisture, and room pressure.

QUANTUM is proficient in designing Clean Rooms to assist with coordinating cycle streams and useful action. We design HVAC systems and Clean Rooms pondering ease of action, viability, backing, and consistency. It emphasizes cutting-edge space use through capable design and a convincing blend.

We design tremendous HVAC systems for plants as well as for R&D centers, Warehouses, corporate working environments and more unobtrusive working environments using VRF.

We follow ASHRAE / SMACNA / EU GMP / ISO 14644 standards and provide following services.
The HVAC framework should be fittingly designed, thinking about the design of the office, with different rooms or areas for capacity of materials and in process materials or items, handling, and development of materials, items and staff. The necessary tidiness classification ought to be accomplished, as well as different boundaries, such as air filtration, wind stream speed, air volumes, pressure differentials, temperature, relative stickiness, suitable and non-feasible molecule counts and regulation. Conditions and cutoff points should be determined, based on need. Makers ought to decide and characterize limits for these. These ought to be reasonable, proper and logically legitimate very still, in activity and as worked at the hour of design. In deciding these, significant factors and dangers ought to be thought of, including yet not restricted to potential disappointments of AHUs, seasonal varieties, properties and kinds of materials and items, quantities of staff and dangers of cross-tainting.
While designing the HVAC system, we consider all parameters and regulations.The parameters are:
  • temperature;
  • relative humidity;
  • supply air quantities;
  •  return air or exhaust air quantities;
  •  room air-change rates;
  •  room pressures and pressure differentials;
  •  airflow pattern;
  •  unidirectional airflow velocities;
  •  containment system velocities;
  •  HEPA filter penetration ;
  •  room particle count ;
  •  duct leakage ;
  •  materials of construction;
  •  microbiological counts;
  •  de-dusting and dust extraction systems.