Cleanroom Editorial and News
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                    Visualizing Airflow With Smoke Studies For Aseptic Manufacturing Excellence
                        7/7/2025
                    
JHS uses smoke studies to visualize airflow in cleanrooms, ensuring aseptic conditions and regulatory compliance for sterile pharmaceutical production, especially on new aseptic filling lines.
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                    Designing Facility Monitoring Systems For Cleanrooms
                        12/4/2023
                    
Let's examine the features and advantages of facility monitoring systems, system architecture considerations, and overall system considerations.
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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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                    Safety Cabinets' Essential Role In EU GMP Annex 1
                        10/25/2024
                    
A new chapter by GMP Compliance Adviser explores safety cabinet classifications and applications, plus requirements for their construction and and installation, per Annex 1.
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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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                    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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                    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.