CLEANROOM VALIDATION

Our Cleanroom Validation services include:

Generation and Execution of IQ/OQ Documentation

Cleanroom Validation in line with ISO 14644 and FED Standard 209E

Cleanroom Validation Feasibility Studies

Validation of Laminar Air Flow Devices

HEPA Filter Integrity / Leak Testing

Airborne Particulate Count Analysis

Environmental Testing including Temperature, Humidity, Noise and Light levels

Airflow Visualisations

KES Validation specialise in providing independent cleanroom validation services for the pharmaceutical, medical devices, semi-conductor and healthcare industries.

Our in-house teams can develop and execute site specific IQ / OQ documentation in line with facility and client requirements and perform hands-on clean room qualification in line with ISO 14644.

KES also perform ongoing Validation which is required to ensure that your cleanroom facility remains within the specified standards.