Cleanroom Validation.
Kantec Engineering specializes in the design, installation, and validation of cleanroom environments across the pharmaceutical, data centre, manufacturing, and research and development sectors. Their expertise spans controlled environment construction, including HVAC system integration, HEPA/ULPA filtration, and laminar airflow solutions to achieve ISO and GMP compliance. Validation services encompass performance qualification (PQ), installation qualification (IQ), and operational qualification (OQ), ensuring that all cleanrooms meet regulatory standards for particulate control, temperature, humidity, and pressure differentials. By combining advanced contamination control methodologies with rigorous testing protocols, Kantec Engineering delivers turnkey cleanroom solutions that support critical processes where precision, sterility, and reliability are paramount.
At Kantec Engineering, we build high-spec cleanrooms that don’t just meet the standard, they define it.
Whether you're starting with a blank slate or upgrading an existing space, we manage everything from concept and design through to build, commissioning, and validation.
Our turnkey solutions are tailored, not templated, because no two environments or requirements are exactly alike. Our in-house validation team takes care of every detail, including performance testing, air balancing, monitoring, and full compliance validation.
We also supply custom-manufactured stainless steel furniture built specifically for cleanroom environments - durable, hygienic, and seamlessly integrated. It’s precision where it counts.
Let's Talk About Your Needs.
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