Your cleanroom, containment suite, or controlled environment must perform precisely as designed, every time. Technickon Ltd provides comprehensive cleanroom validation services to demonstrate compliance with ISO, GMP, MHRA and FDA requirements.
Our engineers ensure that every system, process and environmental parameter performs in line with design intent, regulatory standards and your own internal quality expectations. From installation through operation, we document and verify every step to provide complete assurance of performance and compliance.
We carry out full validation testing and certification for cleanrooms, containment laboratories, and controlled environments.
Our process verifies air change rates, airflow uniformity, temperature and humidity stability, pressure cascades, and particulate cleanliness to the relevant ISO and GMP standards.
Technickon’s validation team provides complete documentation packages, including protocols, reports and certificates.
We support MHRA, FDA and ISO audit compliance, producing clear and traceable documentation that satisfies regulatory bodies and client QA departments alike.
Validation isn’t just a one-time event, it’s an ongoing requirement. We offer routine requalification, revalidation and calibration services to ensure long-term compliance.
We can also assist in corrective validation work following modifications, equipment upgrades, or failed inspections.
Call one of our engineers today to discuss your validation or requalification requirements.
Technickon provides a complete portfolio of cleanroom services designed to ensure your facility performs flawlessly throughout its lifecycle:
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