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Unlike terminally sterilized filled drugs, the stability of the aseptically filled drugs is affected by sterilization methods necessitating an aseptic process to fill certain biologicals, pharmaceuticals, and biotechnology drugs.  Aseptic filling, also known as fill/finish or sterile filling, is a critical process that requires very specific environmental conditions, materials, and controls.

Many factors affect sterile filling including the cleanroom and support facilities, fill/finish equipment, personnel, sterilized filling components, and the sterile product.

Germfree’s bioGO® cleanrooms are pre-designed and adaptive to provide an offsite built, process ready solution for advanced applications, available in 3 primary platform technologies:

Germfree’s advanced process and biosafety equipment is purpose built to meet client user requirements and includes:

·       Class II Biological Safety Cabinets

·        Cleanroom Pass-throughs

·       Laminar Flow Hoods++++

·        Restricted Access Barrier Systems (RABS)

·        Aseptic Isolators

·       Dehumidification Chambers

·        Cleanroom Tables, Shelves, and Workstations 

Speak with an Expert today to learn more about how Germfree can amplify your process.

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Robust Experience

Germfree consistently delivers exceptional Biopharma compliant products around the globe. Browse the grid below to see a selection of relevant past projects:

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