Cleanroom Editorial and News
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The Critical Role Of Training In Cleanroom Cleaning And Disinfection
5/21/2024
Learn why proper training is vital in cleanroom cleaning and disinfection and how to develop and maintain a successful training initiative.
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The Ins And Outs Of Modern Barrier Systems For Sterile Manufacturing
6/10/2024
This article looks at key features of restricted access barrier systems and isolators and discusses some of their applications.
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Balance cGMP And BSL-3 Regulatory Requirements
6/12/2023
Find the right solutions for your organization to comply with and maintain product quality and safety despite conflicting cGMP FDA 21 CFR Part 210 and 211 cleanroom and BMBL requirements.
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Navigating EU GMP Annex 1 Revisions In Drug Manufacturing
11/27/2023
Explore changes introduced by the revised EU GMP Annex 1, key considerations to maintain compliance, and stark statistics that underscore the consequences of non-compliance in this evolving landscape.
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Prioritize Particulate Control For Safer Therapy Development
8/10/2023
As particulate control continues to be a top concern for advanced therapy manufacturers, SUT suppliers must regularly assess every element of the single-use component supply chain.
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Guidance For Pass-Throughs In cGMP Cell And Gene Therapy Facilities
6/12/2023
How do active purging pass-throughs offer a higher level of material control for cell and gene therapy facilities?
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The Very Real Consequences Of Ignoring Cleanroom Residues
3/28/2024
Learn about the problems caused by residues left behind by disinfectant solutions, challenges to residue removal in cleanrooms, and effective removal techniques for ongoing residue management.
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Contamination Control Considerations For Cell And Gene Therapy Facilities
4/17/2023
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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Best Practices For Sterile Fill Operator Gowning Training
4/17/2023
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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Introducing Laminar Airflow Technology In Aseptic Processing
8/21/2023
The global market for injectable drugs will reach $69.13 billion by 2028. Examine the vital role of laminar airflow technology in meeting sterile integrity standards and minimizing contamination risks.