Insights On Pharmaceutical Production

  1. CTS OpTmizer One SFM: Thoughtfully Designed Nutrition For T Cells 5/22/2025

    Learn about a novel, next-generation medium with an animal-component-free formulation developed to support the need for a T-cell medium that allows consistent, reproducible, and automated T-cell manufacturing.

  2. Ingress Leak Test For Bioprocess Containers 5/28/2025

    When a visual inspection with magnification isn't enough, the IPA ingress test can definitively confirm a leak. Learn how to perform this critical quality test.

  3. Visually Clean And Beyond 10/23/2024

    Implement a robust cleaning and sanitization program to ensure the safety and quality of personal care and cosmetics products while complying with global regulations.

  4. Developing A Sterilizing Grade Filter For High Concentration Biologics 7/26/2024

    Explore an approach to developing a sterilizing-grade filter for high-concentration biologics that enabled extensive filterability trials to be conducted without needing a large quantity of product.

  5. What Is A Bowie-Dick Test And Its Importance For Sterility Assurance? 11/26/2025

    Bowie-Dick testing ensures steam sterilizers remove air and achieve full steam penetration. Discover why this simple check is vital for compliance, safety, and preventing costly sterilization failures.

  6. Modern Modeling Tools For Small Molecule Solid Dose Manufacturing 3/10/2025

    Data-driven modeling techniques can enhance scale-up processes, streamline production, and help companies navigate the complexities of modern drug development with greater precision and reliability.

  7. The 5 Key Risks Of Failing To Select The Right CDMO Partner 12/11/2024

    For complex projects involving oral solid dosage (OSD) and sterile drug products, selecting the ideal CDMO can play a pivotal role in determining the success of a drug candidate.

  8. Maximize Operational Readiness And Efficiency Without Compromising Quality 12/12/2025

    Discover how digital transformation drives efficiency, agility, and compliance in pharmaceutical manufacturing to optimize processes, improve quality, and accelerate time-to-market.

  9. Step Inside The Power Of KinetiSol™ 2/26/2026

    Step inside the power of KinetiSol™. This video showcases our KinetiSol Large Scale Commercial Processing Equipment in action, producing amorphous solid dispersions at rates up to 20 kg per hour.

  10. Host Cell Protein (HCP) Removal Post Virus Inactivation In mAb Processing 2/26/2026

    Clarifying post–virus inactivation streams with a charged depth filter can remove precipitates while significantly reducing HCPs. See how a dual‑layer filtration approach supports stronger impurity control.