Our BioPharma Trailers deliver rapid and flexible cGMP cleanrooms, production space, R&D capabilities and biocontainment. These units add capabilities and accelerate “speed to market”. BioPharma Trailers are configured for your required application and can easily be repurposed for biopharmaceutical process change-outs, as Germfree manufactures and inventories all core equipment. We also operate a fleet of mobile cleanrooms that meet FDA cGMP and USP 797/800 requirements. These fully self-contained units are deployed for pharmacy operations and clinical drug trials. Germfree offers rental options to match the duration of your project, including short term applications.
Germfree manufactures complete modular facilities to provide flexible cGMP-compliant production space and R&D laboratories. Our BioPharma Modules incorporate aseptic process areas as well as containment for potent APIs. They are engineered to handle your current requirements and can be reconfigured for future process change-outs. BioPharma Modules are self-contained allowing them to be installed wherever they are needed and without complex on-site infrastructure. We also manufacture turnkey biocontainment labs up to BSL-3 and ABSL-3. Germfree’s BioPharma Modules are manufactured in our controlled factory environment, to deliver an advanced solution in an accelerated timeline.
Germfree designs and manufactures custom Aseptic and Containment Isolators for numerous applications requiring cGMP compliance. We also custom engineer and manufacture Restricted Access Barrier Systems (RABS). Our in-house engineering team works with you to determine the optimal design & process flow, integration of components, properly configured controls and clean air requirements.
Our Unidirectional Airflow Cabinets offer a high degree of localized control for critical aseptic processes. Horizontal and Vertical Laminar Flow Hoods are available. They provide ultra-clean air to enhance sterile product processing, delivering uninterrupted ‘First Air’ to the work zone. We specialize in custom integration of any components and assure that all engineering controls are properly configured for a cGMP-compliant production facility or cleanroom.