Insights On Critical Environments

  1. 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.

  2. ABSL-3 Facility For Duke (National University of Singapore) 6/6/2024

    Read about a 5-module ABSL-3 facility that was constructed in Singapore, and is used for disease surveillance, research on avian influenza, and other risk group 3 materials.

  3. Expanding CDMO Advanced Therapy Manufacturing Capability With BSL-2LS cGMP Facility 6/6/2024

    See how one manufacturer expanded its production capacity with a modular BSL-2LS cGMP facility built to meet evolving CDMO needs while ensuring robust engineering controls and flexible design.

  4. Contamination Control Strategies: Comparing Cleanrooms, RABS, Isolators 10/20/2025

    Sterile manufacturing relies on three main contamination control strategies (CCSs): cleanrooms, RABS, and isolators. Understand how each system compares in sterility assurance, startup cost, and operational flexibility.

  5. Biotech's Plastic Problem Meets Its Match 8/8/2025

    Explore how a partnership with UW–Madison and Genentech developed a breakthrough recycling technology that is poised to reshape single-use bioprocessing sustainability.

  6. Environmental Monitoring Vs. Good Aseptic Technique 4/23/2024

    Review the standards and regulations promoting a cohesive environmental program, and explore manual compounding in laminar flow hoods, through to filling lines, in both open and closed systems.

  7. Mobile Lab For A Large Pharma Client 6/19/2024

    Completed in 2021, learn how this custom BSL-3 mobile laboratory received PHAC approval and ensured a secure environment for PPD powder-related MTech development work.

  8. Overcoming Facility Constraints Posed By Process Intensification 4/14/2025

    Discover how your facility's layout and process flow might limit its potential and learn about media requirements in USP and DSP to optimize your scheduling and footprint for efficient media management.

  9. Monitor Cleanrooms Anytime, Anywhere 8/4/2025

    Remotely monitor cleanroom environments with secure, real-time data access from any device, anywhere, helping to streamline operations and ensure compliance.

  10. A Data-Driven Approach to Cleaning Validation 10/21/2024

    Discover how Ongoing Process Verification, guided by PAT and digital integration, ensures consistent cleaning efficacy, reduces risks, and optimizes production efficiency in the pharmaceutical industry.