Cleanroom Validation Services in Oman

FTS Cleanrooms is a leading provider of cleanroom validation in Oman, delivering precise and reliable cleanroom validation services in Oman for pharmaceutical, biotech, healthcare, and research facilities. Recognized among top cleanroom validation companies in Oman, we offer end-to-end solutions that ensure your cleanrooms, laboratories, and operation theaters meet international standards and local regulatory requirements.
We specialize in cleanroom qualification in Oman and cleanroom requalification in Oman, following ISO 14644 standards, EU GMP guidelines, IEST-RP-CC006.3, and corporate SOPs. Our services ensure your controlled environments maintain optimum cleanliness, airflow, and safety.

Our Cleanroom Validation Services in Oman

Our comprehensive cleanroom validation Oman solutions cover all critical aspects of controlled environments:
Airflow volume and air change rate measurement
Unidirectional airflow velocity verification
HEPA filter integrity test in Oman (DOP and particle count)
Room differential pressure measurement
Non-viable airborne particulate monitoring
Airflow visualization studies
Clean-up recovery tests
Temperature and humidity uniformity mapping
Containment and leak tests
Filter integrity services in Oman for optimal HEPA performance
These tests guarantee that your cleanroom operates efficiently, safely, and in full compliance with ISO and EU GMP standards.

What is Cleanroom Validation?

We provide audit-ready reports that demonstrate your facility meets ISO 14644 standards, EU GMP requirements, and internal corporate protocols. FTS Cleanrooms is the preferred partner for cleanroom validation services in Oman, supporting pharmaceutical, biotech, and healthcare facilities throughout the region.
Cleanroom validation in Oman is the systematic process of documenting tests, procedures, and operational activities to confirm that your cleanroom consistently achieves the required level of cleanliness and compliance.

Validation States: As-Built, At-Rest, Operational

ISO-compliant validation is conducted in three key states:
As-Built:
The cleanroom is empty, without equipment or furniture.
At-Rest:
Equipment and furniture are in place but not in operation.
Operational:
The cleanroom is fully functional, with all processes running.
While many facilities validate only As-Built or At-Rest, we strongly recommend Operational validation, ensuring real-world performance and safety under working conditions.

Standards for ISO 8 Cleanrooms

While many facilities validate only As-Built or At-Rest, we strongly recommend Operational validation, ensuring real-world performance and safety under working conditions.
Correct airflow velocity and volume measurements
Airborne particle counts within allowable limits
Differential air pressure monitoring
HEPA filter integrity testing in Oman and leak verification
Surface contamination monitoring and microbial control
Airflow direction validation
Temperature and relative humidity mapping
Recovery testing for contamination control

Validation States: As-Built, At-Rest, Operational

As one of the leading validation companies in Oman, FTS Cleanrooms offers:
Expertise in cleanroom validation services in Oman
Customized solutions for cleanroom qualification in Oman and cleanroom requalification in Oman
Deep understanding of ISO 14644, EU GMP, and local regulatory standards
Precision testing, including HEPA filter integrity test in Oman and filter integrity services in Oman
Comprehensive support for laboratories, pharma, biotech, and healthcare facilities
Audit-ready documentation and compliance reporting

Partner with Leading Cleanroom Validation Experts in Oman

Choosing FTS Cleanrooms guarantees:
Full compliance with ISO 14644, EU GMP, and corporate standards
Accurate operation theatre validation Oman and HEPA filter testing
Detailed audit-ready reports
Long-term reliability through requalification and operational validation
Get in touch with us today!

FAQs – Cleanroom Validation in Oman

Cleanroom validation in Oman ensures your controlled environment meets ISO, EU GMP, and corporate standards. It verifies airflow, pressure, particulate levels, temperature, humidity, and HEPA filter efficiency, reducing contamination risks and ensuring regulatory compliance.

Facilities generally require annual cleanroom validation services in Oman, but cleanroom requalification in Oman may be necessary after layout changes, new equipment installation, or HEPA filter replacement.

FTS Cleanrooms delivers comprehensive audit-ready reports, including test methods, calibration certificates, results, deviations, corrective actions, and compliance statements, in accordance with ISO 14644 and EU GMP standards.

As-Built checks the empty cleanroom, At-Rest validates installed equipment without operation, and Operational tests the cleanroom under real working conditions. Operational validation, including operation theater validation in Oman, ensures reliable performance.

Cleanroom qualification in Oman confirms a newly constructed or renovated cleanroom meets design standards, while cleanroom validation in Oman monitors ongoing operational performance. Both, including cleanroom requalification in Oman, are essential for regulatory compliance and facility safety.