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:
Mobile (mobile trailer/vehicle platform) Module (self-contained cleanroom module platform) Modular Cleanrooms (integrated, interconnected, multi-module, structural building platform)
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It is the dedication of the Germfree team that enables rapid deployment of critical infrastructure both to cutting edge research facilities and the front lines of global health security
