Cleanroom validation services

This is what we do

We take care of your cleanroom validation

We take care of your ISO and GMP cleanrooms throughout its entire life cycle. After we have started with coordinating and managing your qualification & validation projects, we prepare all of the qualification and validation documents/master plans. On top of that, we carry out a DQ/IQ/OQ/PQ for all of the media, HVAC and process equipment. Once the measurements have been completed, a final check will take place by the ABN Cleanroom Validation engineer. A detailed end report will be handed over to the person in charge of the commissioning party. This measurement report also contains recommendations on how to deal with any comments or deviations.

All our measurements are taken using the most accurate, calibrated measuring devices and our procedures are always in accordance with the current standards. ABN Cleanroom Technology has the experience and knowledge to support you in testing and validation of:

  • Recovery testing
  • Particle deposition testing
  • Temperature & humidity monitoring and uniformity mapping
  • Air tightness testing (RL 10 VCCN)
  • HEPA/ULPA filter integrity testing
  • Areosol photometer method
  • Light-scattering airborne-particle counter method (LSAPC)
  • Non-viable airborne particle monitoring
  • Airflow volume measurements, air change rate calculations and airflow visualization
  • Air Change Effectiveness (ACE) measurements
  • Unidirectional airflow velocity measurements

Still haven't found what you are looking for?

Check out the various services we offer to keep the performance of your cleanroom optimal at all times.

We're happy to support

GET IN TOUCH WITH US

Do you want to receive more information about how pre-engineered building blocks and circular cleanroom design will benefit your project? Simply send over a request. You can also contact us with questions about our services, ranging from cleanroom validation and GMP-monitoring, to commissioning and cleanroom remodeling.

Cleanroom validation services

This is what we do

We take care of your cleanroom validation

We take care of your ISO and GMP cleanrooms throughout its entire life cycle. After we have started with coordinating and managing your qualification & validation projects, we prepare all of the qualification and validation documents/master plans. On top of that, we carry out a DQ/IQ/OQ/PQ for all of the media, HVAC and process equipment. Once the measurements have been completed, a final check will take place by the ABN Cleanroom Validation engineer. A detailed end report will be handed over to the person in charge of the commissioning party. This measurement report also contains recommendations on how to deal with any comments or deviations.

All our measurements are taken using the most accurate, calibrated measuring devices and our procedures are always in accordance with the current standards. ABN Cleanroom Technology has the experience and knowledge to support you in testing and validation of:

  • Recovery testing
  • Particle deposition testing
  • Temperature & humidity monitoring and uniformity mapping
  • Air tightness testing (RL 10 VCCN)
  • HEPA/ULPA filter integrity testing
  • Areosol photometer method
  • Light-scattering airborne-particle counter method (LSAPC)
  • Non-viable airborne particle monitoring
  • Airflow volume measurements, air change rate calculations and airflow visualization
  • Air Change Effectiveness (ACE) measurements
  • Unidirectional airflow velocity measurements

Still haven't found what you are looking for?

Check out the various services we offer to keep the performance of your cleanroom optimal at all times.

We're happy to support

GET IN TOUCH WITH US

Do you want to receive more information about how pre-engineered building blocks and circular cleanroom design will benefit your project? Simply send over a request. You can also contact us with questions about our services, ranging from cleanroom validation and GMP-monitoring, to commissioning and cleanroom remodeling.

1. Off-site production, on-site assembling

Legolisation means standardisation. Standardisation causes a shift in production. Work is carried out in conditioned spaces such as factory halls. our cleanrooms are manufactured partly or entirely off-site, which means huge savings on transport costs and reduction of inconvenience on-site