CLEAN ROOM


clean room

 

Clean rooms in the pharmaceutical industry, hospitals and research institutes are subject to stringent legal requirements regarding room pressure constancy. Insufficient or improperly regulated supply and exhaust air not only causes delicate disruptions in cleanroom operation, but also compromises product quality.

Hospitals

 

In order to minimize the risk of infection in sterile areas and to ensure the necessary hygiene quality, the education, organization and management of the hospital staff, as well as the architectural plan, construction application details and hygienic air conditioning system to prevent cross contamination play an important role.

 

 


Paylaş

 

 

Hospital Clean room

 

In order to minimize the risk of infection in sterile areas and to ensure the necessary hygiene quality, the education, organization and management of the hospital staff, as well as the architectural plan, construction application details and hygienic air conditioning system to prevent cross contamination play an important role.

 

 

 

Pharmaceutical and Sub-Industry Cleanroom

 

In order to protect the product at every stage of the process and present it appropriately to the end user, and to ensure the desired shelf life in the pharmaceutical production and sub-industry, all production stages must be carried out in clean room classes determined according to international standards such as ISO 14644, US FS 209, GMP.

 

Laboratory Cleanroom

 

Sterile air conditioning system architectural plan and construction detail applications have been developed in order to create controlled areas with negative or positive pressure, constant temperature and humidity, according to defined working conditions, in laboratories established to provide R&D or product services in many fields such as pharmaceuticals, chemistry, electronics and optics. .

 

For laboratories with different biological safety levels according to their application areas (BSL-1, BSL-2, BSL-3, BSL-4), special design and project planning should be done by considering international standards. In vitro fertilization (Embryology) laboratories have a separate importance in terms of VOC gases and particle concentration control, and the clinical success rate is directly related to the air quality provided in the environment.

 

Industrial Facilities Clean room

 

Food and sub-industry process design and air conditioning system are extremely important in order to deliver healthy and high quality products to the end user in a sterile and protected manner.

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