Cleanroom Editorial and News
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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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Drug Facility Design For Live Biotherapeutic Products
7/8/2025
Live biotherapeutic products use live microorganisms or yeast as active agents to prevent or treat diseases. For pharma manufacturers entering this emerging field, understanding the unique GMP requirements is critical.
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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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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.
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Best Practices In The Design Of A Pharmaceutical Manufacturing Facility
11/6/2024
A well-designed manufacturing facility is critical to ensuring product quality and regulatory compliance. Let's examine the importance of the concept design review in achieving these goals.
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Advancing Sterile Manufacturing: A Strategic Imperative For Modern Pharmaceutical Production
7/9/2025
Ensuring sterile drug production is vital for patient health and a key regulatory focus. Discover core principles and emerging trends in sterile manufacturing.
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Consumables Are Leading The Cleanroom Market — Here's Why
2/19/2025
As the industry expands, so, too does demand for PPE. This market analysis looks at the trends in consumables and other cleanroom technology used to make medicine.
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EU ANNEX-1 And The Impact Of Contamination Control Strategy On Cleaning & Disinfection
10/21/2024
New EU rules tighten grip on contamination control for sterile drugs. Learn how to ensure your cleaning and disinfection meet the stricter standards.
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Cell And Gene Therapy Facility Design Considerations
6/12/2023
Walk through 20 reasons why it's essential to establish a specialized cleanroom environment specifically tailored for your cell and gene therapy products.