HVAC System Design & Engineering Turnkey Solution

Pharmaceutical GMP HVAC systems are forced-air systems that provide heating and air conditioning as the air circulates through the system. Duct systems, such as central air conditioning, have a central unit that treats the air, and a blower that circulates treated air throughout a building’s ductwork and into the main living space.

Ductless systems like mini-splits do the same thing, but they exchange air directly with the living space instead of through ductwork. As the air passes through the HVAC unit, it may be run through air filters to remove allergens, dust, or other particles.

With the development of GMP, pharmaceutical GMP certification has been implemented internationally. GMP provides the basic guidelines for pharmaceutical production and quality control. Pharmaceutical production must meet the requirements of GMP, and pharmaceutical quality must meet legal standards. Since the implementation of the pharmaceutical GMP system, it has evolved from the initial GMP to cGMP (current Good Manufacturing Practices) to the international GMP standard announced in 2007 (Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme, PIC/S GMP , that is, the EU GMP standard), continuously improving the quality and standards of domestic pharmaceuticals. 

In order to maintain the cleanliness of the air in the manufacturing process or R&D environment, pharmaceutical factories and laboratories often use dust-free sterile rooms to control air quality. In PIC/S GMP, the clean working environment of sterile pharmaceuticals is divided into four levels: A, B, C, and D. Level A refers to local areas of high-risk operations, such as filling areas, rubber stopper storage basins, open ampoules, and vials. and areas for performing aseptic connections, etc., are usually established in the form of laminar flow workstations. Level B area is the background environment of level A area, and level C and D areas are clean areas that perform less critical stages. The cleanliness standards required for various levels of environments are as follows:

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