SteriPharm® is a user and maintenance friendly system providing a cost effective alternative solution for aseptic processing or sterility testing. Available in two standard sizes, SteriPharm® is designed to offer increased protection and quality assurance of process integrity by utilising singe pass turbulent flow ideal for sterility testing or recirculatory unidirectional airflow for aseptic manufacturing process (achieving a Grade A / Iso 5 environment)

  • H2O2 Sensor

    H2O2 Sensor

  • Rapid Transfer Port

    Rapid Transfer Port

  • Viable Sampler

    Viable Sampler

standard containment solutions
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Configured with 2 or 4 glove product handling chambers and the option of entry / exit airlocks.

The on board rapid gassing system enables the operators to handle products in a highly controlled process flow. The SteriPharm® Bio-decontamination process ensures a 6 log reduction in bacterial spore population with inclusive safety features to guarantee operator and plant safety. Increased protection from contamination is achieved by reducing human interventions, physical barrier technology, pressure differential and routine Hydrogen Peroxide Vapour Decontamination.

Design Advantages

Bio Decontamination


Reduction in spore population



Based on empty chamber

Air Clasfication

Iso5 - Grade A

Unidirectional Airflow

Design Advantages

  • Ergonomic design generated by the use of sloping front face, large oval PharmaPort gloveports
  • cGMP compliant design
  • Increased safety by reducing contamination risks (ensuring product compliance)
  • Full process equipment integration within grade A IS05 environment (unidirectional only)
  • Isomon full H2O2 high/low level monitoring, integrated into the control system
  • External H2O2 sensor for room monitoring
  • Safe change filters (UDAF only)
  • Different pressure cascade within each chamber
  • Energy efficient
  • Integrated Hydrogen Peroxide Vapour Decontamination
  • Custom racking and storage to suit the application
  • Space saving design
  • PLC Controlled System with HMI interface

Available Options

  • Millipore Unit fully integrated into isolator base with associated bypass gassing pipework(includes document package)
  • Chart recorder and associated integration costs
  • Viable particle monitoring
  • Non-viable particle monitoring
  • Ø190/Ø270/Ø350 Rapid Transfer Ports

Customer Support

Customer Support

Our planned maintenance and re-certification package provides a scheduled visit to undertake a full range of testing to industry standards.

Service UK: +44 01484 354 499

Service Americas: +1 608-747-2482

Spare Parts Americas: +1 608-747-2475

Technical Requirements

Technical Requirements



SteriPharm® Isolator Overall Height Overall Depth Overall Width Chamber Width Chamber Depth Chamber Height
4 Glove with Airlock (Turbulent) 2320mm – 91⅜” 880mm – 34⅝” 3180mm – 125⅕” 1840mm – 72½” 600m – 23⅝” 850mm – 33½”
4 Glove single chamber (Turbulent) 2320mm – 91⅜” 880mm – 34⅝” 1850mm – 72⅘” 1840mm – 72½” 600m – 23⅝” 850mm – 33½”
4 Glove with Airlock (UDAF) 2475mm – 97½” 1219mm – 48” 3180mm – 125⅕” 1840mm – 72½” 740m – 29⅛” 850mm – 33½”

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