Cleanroom Whitepapers and Case Studies

  1. Emergency Containment Solutions And Disaster Support For A Liquid Storage Facility 5/12/2023

    Discover how a successful partnership between an environmental company and a liquid storage facility helped mitigate a disaster from escalating and gave them the rapid response they needed. 

  2. Improve Your Molecular Cloning Process With Synthetic Biology Automation 5/25/2023

    Explore the promising field of synthetic biology, the hurdles manufacturers face with it's workflow, and how automation can help accelerating throughput and walkaway time.

  3. Leaks Go Acoustic: How Rogers Water Reduced Waste And Built Resiliency 10/1/2024

    Read how Rogers Water Utility (RWU) took action to mitigate constant leaks in their distribution system, which made it challenging to maintain volume in the eastern district’s water tower.

  4. Prefabricated Viral Vector Modular BSL-2LS cGMP Facility In 13 Months 6/26/2024

    Learn about the modular BSL-2LS cGMP facility that was constructed to support 3 processing lines for German-based CDMO Vibalogics as the company sought to expand in the U.S. market for viral vectors.

  5. From Open Cleanrooms To Closed Systems – What Is Driving The Change? 3/14/2025

    Aseptic processing is evolving. Regulatory changes and technological advancements are driving a shift from open cleanrooms to closed systems for sterile drug manufacturing.

  6. Calcium Carbonate Vs Titanium Dioxide: Why Particle Engineering Matter 11/10/2025

    Discover how particle-engineered calcium carbonate offers a viable alternative to titanium dioxide in tablet coatings, achieving good opacity, process efficiency, and comparable tablet properties.

  7. Solving The Silicone Challenge In Pre-Fillable Syringes 8/27/2024

    Discover a technology platform that is revolutionizing the pre-fillable syringe market by solving the challenge of silicone sensitivity, ensuring stability for sensitive drugs.

  8. Buffers And Process Liquids For Biopharmaceutical Production: Considerations For Scale-Up And Outsourcing 5/7/2024

    For small and midsize biopharmaceutical organizations, outsourcing buffer and process liquid preparation, quality testing, and storage could significantly streamline operations and reduce regulatory risk.

  9. Enhancing Viral Clearance Prediction And Process Optimization 7/11/2025

    MockV technology enables early, in-house viral clearance assessment, helping biopharma developers improve process robustness, reduce costs, and enhance safety before GMP manufacturing begins.

  10. Navigating Regulatory Compliance: A Success Story In The Pharma Industry 4/10/2025

    Reveal how one pharmaceutical facility overcame strict cross-contamination rules and space limits without costly building modifications to ensure operational continuity.