LAF Tech has expanded its cleanroom validation services across Australia, adding capacity to support pharmaceutical, biotechnology, healthcare and scientific research facilities.
The expanded service range includes cleanroom commissioning, installation and operational qualification (IQ/OQ), requalification and ongoing validation of controlled environments.
Environmental monitoring, calibration and performance testing services have also been extended to support a wider range of cleanroom validation work.
The services are used to support compliance with Good Manufacturing Practice (GMP) requirements and other regulatory standards covering contamination control and environmental performance.
LAF Tech’s validation activities include particle counting, airflow and pressure differential testing, microbial monitoring and sensor-based data collection in cleanroom and laboratory environments.
The services are used on both new facilities and existing sites across Australia that are undergoing scheduled revalidation.
Recently, the company delivered environmental monitoring systems for AdvanCell’s radiopharmaceutical facility in Sydney and partnered with cleanroom containment expert, Block Technology, on the installation of vaporised hydrogen peroxide (VHP) decontamination chambers at a GMP vaccine manufacturing site in Melbourne.
Image credit: LAFTech