Innovating Cleanroom Excellence
Validation, or regulatory compliance, remains indispensable in industries like pharmaceuticals, medical implants, semiconductors, space, defence, biotechnology, and food manufacturing. It ensures that cleanrooms and HVAC systems meet the toughest design, installation, operational, and performance standards.
As an organisation of repute in the line, we at Kaizen Airtreat know what it is to design and manufacture validated and certified cleanrooms, be it for new or existing setups.
It includes within itself Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ). A collaborative effort contains the steps mentioned below.
Undertaken mainly through manufacturers and developers, it is done to ensure that the design meets real-world specifications.
These involve end-users and their qualified personnel verifying the installation for its functionality and performance.
Routine assessments at fixed intervals that assure the system adheres to established standards.
Detailed documentation to provide transparency and support regulatory compliance.
We specialise in providing Turnkey Solutions, including Designing, Engineering, Procurement, Construction, Commissioning, Validation, and FEED services, including operation & maintenance of cleanroom and HVAC systems that cater to diverse industries such as Automotives, EVs, Semiconductors, Pharmaceuticals, Healthcare and Medical, Electronics, Aerospace, and the Food industry.
We specialise in providing Turnkey Solutions, including Designing, Engineering, Procurement, Construction, Commissioning, Validation, and FEED services, including operation & maintenance of cleanroom and HVAC systems that cater to diverse industries such as Automotives, EVs, Semiconductors, Pharmaceuticals, Healthcare and Medical, Electronics, Aerospace, and the Food industry.