Insights On Critical Environments

  1. 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.

  2. Tour Of Germfree's bioGO® Mobile cGMP Cleanroom 4/12/2024

    Go step by step through a cleanroom with cutting-edge features and functionalities of our Mobile Cleanroom, which offers a flexible solution for aseptic processing needs.

  3. The Critical Role Of Residue Removal In Cleanroom Biosafety Cabinets 3/28/2024

    Learn about the significance of residue removal, how it is effectively performed in cleanrooms to ensure the compliance of biosafety cabinets, and the impact of proper residue removal.

  4. Scope 3 Emissions: Cut The Complexity With Creative Collaboration 11/20/2024

    Delve into the crucial role of Scope 3 emissions in the biopharma industry's sustainability journey, and learn more about the challenges and opportunities of managing these types of emissions.

  5. Strategic Space Management 8/23/2024

    A pharmaceutical company facing storage space issues decided to outsource its reference samples to Q1 Scientific, a stability storage service provider, resulting in cost savings.

  6. Airflow Visualization Studies: The Impact Of Annex 1 On Sterility Assurance 12/18/2024

    Airflow visualization techniques like Smoke Studies and CFD analyses are crucial for contamination control, aiding cleanroom qualification, environmental monitoring, and optimizing contamination control strategies under Annex 1.

  7. Driving Continuous Improvement: Pushing Through The Barriers To Change 10/15/2024

    Discover how continuous improvement drives efficiency in pharmaceutical manufacturing. Learn strategies to harmonize processes and reduce environmental impact in this thoughtful exploration.

  8. 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.

  9. PUPSIT Without The Pain: Practical Solutions For Implementation 5/6/2025

    Explore the critical role of pre-use post-sterilization integrity testing in quality risk management, as well as learn about integrity testing, wetting procedures, and innovative filtration systems for effective implementation.

  10. Thermo Fisher Scientific Large Volume Liquid Expansion 5/2/2024

    This video provides an insightful look into the expansion of the large volume liquids manufacturing site at the Grand Island facility, highlighting the various stages of the manufacturing process and the capabilities it offers to support the bioprocessing industry.