Insights On Critical Environments

  1. A Biosafety Cabinet For Virology Studies And Disease Surveillance 6/19/2024

    Discover how Germfree tackled a unique challenge from the Public Health Agency of Canada by designing a custom Class III biosafety cabinet for advanced virology studies and disease surveillance.

  2. Unstoppable Critical Cleaning To Increase Pharmaceutical Throughput 5/20/2024

    Process optimization is key to achieving effective pharmaceutical and cosmetic critical cleaning. Learn how manufacturers can improve cleaning efficiency and ensure product safety.

  3. From Concept To Creation: An Inside Look At Engineering Design 4/12/2024

    Step into the world of cutting-edge design and engineering proficiency of the BSL-3 cGMP Modular Facility.

  4. Do Not Bear Cross Contamination In The Pharmaceutical Industry – Prevent It 3/25/2025

    Learn how thorough cleaning and process optimization in pharma manufacturing prevent cross-contamination, ensure product integrity, and enhance efficiency while also improving compliance and reducing costs.

  5. Avoiding IT Outages With Continuous Cleanroom Monitoring Technology 8/13/2024

    Examine how one environmental monitoring system provided seamless and continuous cleanroom monitoring and control during the major global IT outages due to the CrowdStrike incident.

  6. Detection Of Low-Level Bacterial Contamination Using ICR Swabs And Contact Plates 9/22/2023

    Contact plates and swabs are commonly used for surface monitoring in aseptic manufacturing. Here, we demonstrate the recovery rates of MilliporeSigma’s ICR Swabs and lockable TSA w. LTHThio contact plates.

  7. How Crucial Is Culture Media Selection In Environmental Monitoring? 6/20/2023

    Explore culture media regulatory requirements, the impact of manufacturing guidelines and media features and specifications on environmental monitoring, and the importance of media supplier selection.

  8. Applying Appropriate Limits In Cleanroom Monitoring 6/18/2024

    Explore ISO 14644-1:2015 and EU GMP Annex 1 in-depth, and learn about cleanroom classification, how to apply monitoring limits in cleanroom environments, and more.

  9. Why Compounding Pharma Manufacturers Should Evaluate BFS Systems 12/5/2024

    Discover how BFS technology offers compounding pharmacies and 503B facilities enhanced sterility, reduced errors, cost savings, and superior product integrity for aseptic pharmaceutical manufacturing.

  10. Characteristics Of Environmental Residues And Protocols For Removal 4/1/2025

    Examine disinfectant residue characteristics, impacts, and removal challenges in cleanrooms, as well as learn about the practical requirements for maintaining cleanliness standards and addressing these residues effectively.