Cleanroom Products

  1. High Speed In-Line HVLD For Pre-Filled Syringes 10/14/2022

    HVLD is High Voltage Leak Detection, a sensitive, non-destructive technology to test container closure integrity in a variety of liquid-filled pharmaceutical and medical containers including glass vials and ampoules, IV-bags, Blow Fill Seal (BFS) bottles and cards and pre-filled syringes. HVLD can be used to conduct CCIT on any liquid-filled product as long as the container is made of electrically insulated material and it contains an electrically conductive solution.

  2. GMP Services To Support Commercial Development 5/30/2024

    Expedite your development with our comprehensive suite of GMP services specifically designed to streamline regulatory and get you to market faster.

  3. bioGO® 53' Mobile Containment Laboratory 11/3/2022

    Germfree’s bioGO® Mobile Biocontainment Laboratories offer the ideal solution for providing surge capacity for laboratory services during periods of emergency. By utilizing a fully equipped/turnkey Mobile Biocontainment Laboratory, facilities are able to rapidly increase their volume without sacrificing capabilities. Each mobile facility is engineered and constructed to meet or exceed relevant CDC NIH BMBL 5th Edition and World Health Organization (WHO) guidelines for BSL2, 2+, or 3 laboratories.

  4. Cleanrooms And Equipment For Cell Therapy Drug Manufacturing 6/9/2023

    Delivering on the promise of cell and gene therapy through Germfree products and services.

    Germfree Laboratories offer advanced modular and mobile facilities, equipment, and comprehensive services for cell therapy manufacturing. Acknowledging the complexity of personalized treatments, Germfree’s adaptable solutions optimize production processes, ensuring aseptic conditions, scalability, and compliance with regulatory standards. This enables efficient, high-quality cell therapy delivery to patients in need, supporting manufacturers in overcoming industry challenges.

  5. Linear Stage With The Highest Force And Precision: N-332 7/31/2024

    The N-332 linear stage, powered by PICMAWalk, the longest-lasting piezo-motorized drive principle on the market, delivers an impressive 75 N active force with a 3 nm minimum incremental motion.

  6. Class II Pharmaceutical Biosafety Cabinets 11/3/2022

    Germfree is internationally recognized as a leading manufacturer of Class II Biological Safety Cabinets. Our Class II Gloveboxes provide containment for diverse research applications in advanced biopharma laboratories. Our Class II BSCs are engineered to exceedingly rigorous standards for work that requires the protection of operator or product. We specialize in custom integration of all laboratory components.

  7. Class 2 Biological Safety Cabinet 8/29/2023

    The Class 2, Type A2 Laminar Flow Biosafety Cabinet provides a high degree of localized protection from particulate and aerosol hazards. The work area of the biological safety cabinet is continuously bathed with laminar flow ISO 5 HEPA-filtered air to protect the product from contamination while an inward airflow protects the user. Approximately 70% of the air from each cycle is recirculated through the supply HEPA filter while the remaining air is discharged from the biosafety cabinet through the exhaust HEPA filter. These biosafety cabinets eliminate cross-contamination and the accidental release of carcinogenic aerosols and drugs to the outside environment.

  8. AAV Manufacturing With Advanced Polymer And Lipid Technologies 9/23/2024

    By combining purpose-built polymers and lipids, animal-origin-free reagents seamlessly blend into the AAV manufacturing process during transfection to dramatically increase AAV titers.

  9. Pharmaceutical Cleanroom Flooring 8/10/2020

    Floor to Wall Integration at Airwall Corridor.

  10. Automated, Single-Use System For Clinical And Commercial LNP Production 7/21/2023

    The NanoAssemblr® commercial formulation system is an automated, single-use system for the clinical and commercial production of lipid nanoparticles (LNPs) under cGMP conditions. Designed for efficient changeover and robust manufacturing processes, the system enables operational flexibility and standardized manufacturing of genomic medicines.