Insights On Critical Environments

  1. 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.

  2. Normalized Data In Microbial Continuous Monitoring 7/24/2025

    Learn how EU GMP Annex 1 (2022) redefines cleanroom air monitoring standards and emphasizes continuous viable sampling in Grade A and B environments to ensure aseptic integrity and compliance.

  3. Embarking On A Successful Cleanroom Project: Conception To Delivery 6/26/2024

    Learn how you can obtain comprehensive solutions for cleanroom projects that help you ensure regulatory compliance and operational efficiency.

  4. AI Predictive Maintenance Prevents Batch Loss And Production Shutdown 8/5/2025

    AI-powered predictive maintenance with wireless vibration sensors prevented costly batch loss and production shutdowns in pharma manufacturing by detecting and fixing equipment issues before failures occurred.

  5. Monitoring Compressed Gases For Microbial And Particle Contamination 2/26/2025

    There are several factors associated with active environmental microbial monitoring. Watch to learn how the EU GMP Annex 1 compliance focuses on microbial monitoring in cleanrooms.

  6. 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.

  7. Nitrosamines - New Requirements To Evaluate Contamination Risks 12/23/2024

    Explore nitrosamine contamination, regulatory actions, and new evaluation requirements, featuring expert insights from Dr. Ulrich Reichert on prevention and risk assessment strategies.

  8. Optimizing Microbial Air Sampling To Reduce False Positives In Cleanrooms 10/18/2024

    Learn how modern advancements can improve the efficiency of microbial air sampling while minimizing the chances of false positives in cleanrooms.

  9. Establishing Effective Visual Residue Limits In Cleaning Validation 10/23/2024

    Learn about the technical nuances of Visual Residue Limits (VRLs) determination and explore strategies to implement robust VRL programs that meet regulatory standards and enhance manufacturing efficiency.

  10. BSL-3 cGMP Modular Facility Tour 4/12/2024

    Walkthrough the BSL-3 cGMP Modular Facility and learn about how its features deliver top-tier solutions in biosafety and pharmaceutical manufacturing.