Visit our Virtual Process Space for an interactive demonstration!

Mail icon

Aseptic Split Butterfly Valve 10-6 Sterility Assurance

AseptiSafe® Bio Transfer Valve

___

ChargePoint Technology’s sterile powder transfer valves offer increased sterility assurance when handling sensitive ingredients and small components in fill/finish aseptic processing and biotech sterile API production.

The ChargePoint AseptiSafe® Bio valve performs aseptic transfers that maintain critical area integrity with an SAL of up to 10-6.

Left arrow Right arrow
technician locking an aseptic split butterfly valve
aseptic transfer valve
close up of aseptic valve technology
aseptic valve cross-section
a technician opening an aseptic split butterfly valve
aseptisafe bio aseptic valve
the contents of an aseptic valve being analysed
technician locking an aseptic split butterfly valve
aseptic transfer valve
close up of aseptic valve technology
aseptic valve cross-section
a technician opening an aseptic split butterfly valve
aseptisafe bio aseptic valve
the contents of an aseptic valve being analysed

Product information

ChargePoint’s industry leading, patented AseptiSafe Bio valve uses an enhanced decontamination step in the aseptic split butterfly valve process to provide a validated 6 log reduction.

During the powder transfer process, using the aseptic valve and before the product is transferred, the disc faces of the AseptiSafe Bio valve are exposed to decontamination gases within a sealed chamber to ensure decontamination of all critical areas killing organisms effectively and quickly whilst protecting the product from the decontamination gases.

ChargePoint AseptiSafe® bio valve:

  • Is compatible with SIP (steam in place) and H2O2 Biodecontamination sterilisation methods
  • Can eliminate the need to construct large high air class control areas in new facilities
  • Has an optimised biodecontamination cycle
  • Is ideal for lower grade cleanrooms to reduce the costs associated with the construction, validation and management of large clean areas

The active unit is sterilised in place with the use of a SIP Passive unit.

The two aseptic valve halves are docked together.

The disc faces are exposed to decontamination gases within a sealed chamber prior to the product transfer to ensure decontamination of critical areas.

The active unit is the driving half of the valve. Once operated the disc will open to allow the transfer of material through the valve. The active and passive interface is sealed to ensure no material can penetrate the critical area. Once the transfer has taken place the valve is closed.

The active and passive units are then unlocked and undocked revealing the previously closed interfaces ensuring a clean transfer.

  • Overview

    ChargePoint’s industry leading, patented AseptiSafe Bio valve uses an enhanced decontamination step in the aseptic split butterfly valve process to provide a validated 6 log reduction.

    During the powder transfer process, using the aseptic valve and before the product is transferred, the disc faces of the AseptiSafe Bio valve are exposed to decontamination gases within a sealed chamber to ensure decontamination of all critical areas killing organisms effectively and quickly whilst protecting the product from the decontamination gases.

    ChargePoint AseptiSafe® bio valve:

    • Is compatible with SIP (steam in place) and H2O2 Biodecontamination sterilisation methods
    • Can eliminate the need to construct large high air class control areas in new facilities
    • Has an optimised biodecontamination cycle
    • Is ideal for lower grade cleanrooms to reduce the costs associated with the construction, validation and management of large clean areas
  • How it works

    The active unit is sterilised in place with the use of a SIP Passive unit.

    The two aseptic valve halves are docked together.

    The disc faces are exposed to decontamination gases within a sealed chamber prior to the product transfer to ensure decontamination of critical areas.

    The active unit is the driving half of the valve. Once operated the disc will open to allow the transfer of material through the valve. The active and passive interface is sealed to ensure no material can penetrate the critical area. Once the transfer has taken place the valve is closed.

    The active and passive units are then unlocked and undocked revealing the previously closed interfaces ensuring a clean transfer.

  • Specifications

  • Product video
  • Related products