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.
Cleanroom Validation Projects: