
ABOUT GERMFREE
Germfree manufactures a comprehensive line of barrier systems for aseptic control and containment as well as a complete mobile and modular cGMP facilities. We offer advanced solutions to maintain cGMP processes and production for a wide range of biopharmaceutical applications. We are a single source OEM provider of complete cleanroom and lab facilities, and the corresponding integrated equipment designed an purpose-built by our leading-edge fabrication technology, engineering teams and subject-matter experts.
CONTACT INFORMATION
Germfree
4 Sunshine Blvd
Ormond Beach, FL 32174
UNITED STATES
Phone: (386) 265-4360
FEATURED ARTICLES
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Compare and contrast the different construction methods available for designing and constructing a cleanroom, including stick-built construction, modular panels, prefabricated modules, and mobile cleanrooms on wheels.
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Find the right solutions for your organization to comply and maintain product quality and safety despite conflicting cGMP FDA 21 CFR Part 210 and 211 cleanroom and BMBL requirements.
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Here, we compare and contrast horizontal and vertical airflow hoods and discuss their applications and benefits in the pharmaceutical and compounding industries.
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How do active purging pass-throughs offer a higher level of material control for cell and gene therapy facilities?
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Walk through 20 reasons why it's essential to establish a specialized cleanroom environment specifically tailored for your cell and gene therapy products.
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Delve into the key factors determining the flow, the influence of cleanroom classification, a hybrid approach to flow systems, and the advantages of some cleanroom pass-throughs.
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Compare and contrast the pros and cons of several cleanroom design and construction methods to determine the most suitable approach for your specific cleanroom project.
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Review the process requirements, workflows, and process interventions that are key to your containment isolators achieving compliance with both cGMP and BSL-3.
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Gain a thorough understanding of active HEPA purging pass-throughs along with the numerous benefits associated with their use in cell and gene therapy facilities for material control.
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Sterile fill operators are crucial in ensuring pharmaceutical products are contaminant-free and safe for use. Explore best practices for sterile fill operator gowning training, mobile cleanroom benefits, and more.
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A global EPCMV firm worked closely with a cleanroom vendor to deliver a manufacturing facility that meets guidelines for BSL2–Large Scale. Learn about the facility, companies involved, and more.
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Explore the essential components of cleanroom design necessary for Category 2 drugs to adhere to the updated stipulations within USP 797 / 800 chapters.