Clean Room and HVAC Validation

Co-So India perform the room cleaning and HVAC complying the relevant standards ISO 14644-1,2,3, EU GMP/EC GMP. FS 209E, WHO 20020, USFDA, MHRA, Drug and Cosmetic Act of India,2005.

Co-So India provides Clean Room and Area Validation services with complete set of latest equipment’s by experienced engineers. Our primary area of quality service is fulfilling  validation, regulatory and compliance services from stand-alone automated equipment to start-up, commissioning and validation of new facilities by complying relevant standards ISO 14644-1,2,3, EU GMP/EC GMP . FS 209E, WHO 20020, USFDA, MHRA, Drug and Cosmetic Act of India,2005.

Services offered for Cleanroom and HVAC Validation

Cleanroom Validation/HVAC Validation is performed for a variety of reasons. To ensure that the design of the facility is fit for its intended purpose; to ensure that the facility, equipment, and environment meets User Requirement Specifications (URS); to ensure that the facility, equipment, and environment meet defined regulatory requirements; to ensure that the facility, equipment, and its environment function together as a system to meet defined standards.

Co- So India specializes in providing our customers in the Pharmaceuticals, Biotechnology & Medical devices, Operation Theaters , Pathology Laboratories , Research and Production Facilities and cleanroom facilities available in other industries.

Our Cleanroom and HVAC Services includes

Looking For an Experts in Clean Room Service?

Co-So India Techno Solutions, an Assured Environment validation Services is the One stop Best in Class Cleanroom and HVAC Validation Service Providers for Pharma, Healthcare, Food and Beverages.

We meet certifications and compliance needs as per ISO Standards: ISO 14644-1,2,3, EU GMP/EC GMP, FS 209E, WHO, USFDA, MHRA & Drug & Cosmetic Act of India,2005.

Our primary focus is Quality, Regulatory & Compliance Services focused on “Think Green Breath Clean” Module