Cleanroom Qualification

Ensuring Your Facility Meets Every Regulatory & Operational Requirement

Once a cleanroom or controlled environment is built, it is essential to prove it operates as intended and meets all regulatory and user requirements.

Technickon provides comprehensive cleanroom qualification services, documenting and verifying every aspect of design, installation, operation, and performance to give you complete peace of mind.

Whether your facility is newly built, upgraded, or supplied by another contractor, our system ensures full compliance and operational reliability.

Comprehensive In-House Qualification System

Our engineers use a robust, in-house qualification system to plan, execute, and document every stage of the process.

This system has been adopted as a model by QA departments in the pharmaceutical industry and ensures that all regulatory and operational requirements are clearly met and verifiable.

Expert Engineers & Regulatory Knowledge

Technickon’s engineers combine technical expertise with a deep understanding of regulations, GMP standards, and cleanroom systems.

Attention to detail ensures that every test, measurement, and validation step is accurate, reliable, and fully compliant, giving clients confidence in facility performance.

Transparent, Collaborative Process

We involve key personnel from your team at every stage, ensuring complete transparency and agreement before moving forward.

Our service can also be delivered independently for facilities or systems built by other contractors, providing an impartial verification of compliance and operational effectiveness.