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Clean room technology has become essential for the global market players in pharmaceutical industry. Hemair goes beyond providing robust clear rooms with energy wise operating systems. We are capable of designing, supply of equipment, accessories in relate to the HVAC and environments, installation at site, commissiong, testing and providing the necessary certification and validation documents in order to meet various cGMP regulatory requirements. Environment free of bacteria, viruses, or other pathogens in addition to the temperature and humidity controlled work area is must for quality output. Hemair provides its customers all such data and information at the conceptual stage of the project. We have been partnering with the client, in keeping the system in validated mode by maintaining and certifying the system on regular basis.
"Cleanroom standard ISO 14644-1 specifies a ' A room in which the concentration of airborne particles is controlled, and which is constructed and used in a manner to minimize the introduction, generation, and retention of particles inside the room and in which other relevant parameters like temperature, humidity, and pressure, are controlled as necessary." Hemair has been in forefront in bringing these technologies in a cost effective manner. |
