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    Cleanrooms are the enclosed, classified spaces used for processing bio/pharmaceuticals in a contained space with controlled reduction of airborne particulates, including microbes. Virtually every facility producing biologics or pharmaceuticals has at least one cleanroom. Here you will find information about cleanroom design, construction, operation and regulations.

    Articles

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    The pharma industry is running out of lab and manufacturing space — but there are options
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    With regulators revising policies to provide clarity around best practices for aseptic manufacturing, cleanrooms are evolving
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    Early planning will ensure pharma facilities meet requirements
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    Raising the importance of hygiene in accelerated vaccine manufacturing
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    Rapid Transfer Systems have become a popular method of transferring items in an era where containment systems are needed more than ever
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    Pharma entrepreneurs often have to choose between building their own facilities or outsourcing discoveries — but could there be a middle ground?
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    Electronic monitoring of biological safety cabinets supports aseptic processes and cGMP compliance
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    Particle analysis methods and ISO 8573 Standard updates
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    Innovations that make life easier in the cleanroom
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    Pre-fab and modular cleanrooms are on the rise, but stick-built still dominate.
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    How the use of aseptic split butterfly valve technology can prevent contamination
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    Revised GMP guidelines will strengthen emphasis on contamination control, impacting cleanroom performance qualifications
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    How the pharma industry's big ideas are impacting sterile manufacturing