OUR CAPABILITY
Vilair-AAF in Association with Advance Filtration Services is a specialist supplier of laminar airflow and powder containment equipment for high technology
manufacturing. Our modular systems are engineered to meet the needs of any application that requires
ultra-clean air or containment of hazardous aerosols.
Our aim is to provide highly cost-effective equipment solutions that meet stringent industry and government
regulations. We have designed, manufactured and installed purpose-engineered systems for Australia’s
leading manufacturers of pharmaceuticals and medical devices.
APPLICATIONS
Many critical applications in the biopharma and related high technology industries require process environments such as
cleanrooms or enclosures that control levels of particulate or biological contamination. Typical requirements include
laminar flow ultra-clean zones and clean rooms for production of sterile therapeutic goods; and dispensary containment
booths for protection of process workers from potentially hazardous powders.
EQUIPMENT
Our modular designs are adaptable to meet a wide range of specific
site requirements. This approach provides specifiers with the
flexibility to achieve optimal configuration of the clean air system
and process equipment. The modular concept allows subsequent
expansion or relocation without significant costs and downtime.
Stringent equipment specifications include pharmaceutical-grade
stainless steel finish and low levels of noise and vibration. As the
Australian distributor for American Air Filters® (AAF®) – the world’s
largest air manufacturer of air filters - we have online access to
world-class cleanroom technologies, research and support. High-quality AAF HEPA or ULPA filters and framing systems,
together with appropriate fan selection ensure continuing achievement of specified performance criteria. On larger units,
a proprietary monitoring and alarm system provides operators with a continuous indication of airflow in critical zones.
PROJECT MANAGEMENT
We recognise the importance of project completion to agreed specifications, time schedules and costs. Installation of our
systems is effectively managed from project commencement to commissioning and validation.
COMPLIANCE
We understand the requirements of Australian standards and government regulatory codes, such as those for
manufacture of sterile medicinal products and devices. Our systems are designed, manufactured and installed in
accordance with relevant Australian and international standards. Validation of installations is confirmed by independent
NATA-accredited testing and certification.
U L T R A - C L E A N E N V I R O N M E N T S I F O R T H E B I O P H A R M A I N D U S T R Y
