Cleanroom Editorial and News

  1. 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.

  2. 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.

  3. 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.

  4. 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.

  5. Integrating Smart Building Management And IoT Technologies In Biopharmaceutical Cleanrooms 12/19/2025

    IoT-enabled smart BMS modernize biopharmaceutical cleanrooms through continuous monitoring, predictive analytics, energy efficiency, and strengthened regulatory compliance, enabling safer, more efficient operations.

  6. 0.45 m/s ±20% At Working Position In Closed Sterility Testing Isolators: Requirement Or Convention? 2/19/2026

    Balance compliance and efficiency in sterility testing. Explore how a risk-based approach to airflow and isolator technology aligns with Annex 1 while optimizing contamination control.

  7. Elevating Environmental Monitoring Trending: From Data To Insight 2/12/2026

    Move beyond raw data by using heat maps and site-specific limits to identify contamination hotspots. Transform your environmental monitoring into a proactive strategy for operational excellence.

  8. Adapting To Evolving Needs: How Modular Cleanrooms Enhance Safety In Pharmaceutical Manufacturing 6/9/2026

    High-potency therapies demand stringent containment and worker safety. Discover how scalable, modular infrastructure simplifies compliance and protects product integrity in regulated facilities.

  9. 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.

  10. 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.