Based in California, we pride ourselves on being pioneers. The ARS Frontier 2000™ cGMP PLC sterilizer control system is a descendant of the Frontier system first introduced by ARS in the early 1980's. Our control systems have always incorporated independent watchdog recorders to insure that the controlling devices are operating within normal specifications. We guarantee that our systems will control temperature in the pressure vessel to ± 0.5°C or less. We custom build each unit to order and engineer each to your requirements. Cycles include gravity, vacuum (pre-, post- or both), air-over-pressure with our without mechanical mixing or cascading water, rapid cooling or any combination you specify. For exceptional value, we will custom build a new cGMP sterilizer using a refurbished pressure vessel. To back up our superior quality claim, we offer a two-year parts and labor warranty, extendible up to five years with up to fifteen years on pressure vessels (see ARS warranty for details).

To compliment our line of cGMP sterilizers, we offer steam generators built by Electro-Steam Generator Corp., RO/DI water systems by Glegg Water Conditioning, laboratory water stills and sterilizers by Consolidated, ultrasonic cleaners by Sonic Systems, Inc., glassware, cage and cart washers by Buxton, a complete line of life sciences and general laboratory equipment by Boekel and directly offer field repair, maintenance and calibration services by our own Autoclave Repair Specialists (ARS).

Custom built just for you.

GMP only has specific meaning within your facility, in your manufacturing process and for your specific products. The requirements for terminally sterilized large volume parenteral drugs are radically different from a sterile fill biopharmaceutical drug. An ARS sales engineer or dealer will review your sterilization application and work with you to define precisely what you need. Any size, any cycle from simple gravity displacement to more sophisticated rainingCustom built just for you. GMP only has specific meaning within your facility, in your manufacturing process and for your specific products. The requirements for terminally sterilized large volume parenteral drugs are radically different from a sterile fill biopharmaceutical drug. An ARS sales engineer or dealer will review your sterilization application and work with you to define precisely what you need. Any size, any cycle from simple gravity displacement to more sophisticated raining water cycles, with state-of-the-art PLC based controls, with all 316/316L stainless steel chambers or refurbished nickle clad chambers, with manual hinged doors or power sliding doors, we can do it, just for you.