Insights On Liquid Dose Manufacturing

  1. Maximize Quality Assurance Through Rapid Sterility Testing 9/10/2024

    This webinar explores mitigating the risk of product loss, and production delays, as well as the critical role rapid sterility testing plays in ensuring the quality and safety of cell therapy products.

  2. Sterility Testing Of Products With Antimicrobial Properties 6/4/2024

    Drugs formulated with antibiotics, preservatives, or other chemicals may inhibit microbial viability and growth. Learn more about three golden rules to be effective against antimicrobial effects.

  3. De-Risking The Transition From Vial To Drug-Device Combination Product 7/25/2025

    When transitioning from a vial to a combination product system, the best approach is to have a holistic de-risk strategy with an intentional focus on the patient, the plan, and the product.

  4. Driving Excellence In Aseptic Fill-Finish: A Strategic Partnership With Stäubli Robotics 5/29/2025

    See how intelligent automation and purpose-built robotics deliver contamination control and operational excellence in demanding sterile manufacturing environments.

  5. Headspace Gas Ingress Methods: A Key Solution For CCIT 12/23/2024

    Gain insight into the development and validation of headspace methods for various product-container configurations with Dr. Derek Duncan and MSc, Josine Wilmer.

  6. What Does Annex 1 Mean For Cryovial Filling? 10/6/2025

    New sterile manufacturing rules require major changes to cryovial filling. Ensure compliance by adopting better "first-air" protection, minimizing human contact, and using 100% dose checks.

  7. Automated Production Line For Vial Filling And Crimping – A Case Study 4/16/2025

    Discover how a leading pharmaceutical manufacturer overcame space constraints and regulatory requirements to increase vial filling and crimping capacity through a custom-designed automated system.

  8. Fluid Management Strategies For Scalable Biopharmaceutical Production 4/16/2025

    Effective fluid management systems are indispensable in therapeutic manufacturing. Discover how modular design, automation, and single-use systems enhance scalability and maintain product integrity.

  9. A Standardized Gloveless Robotic Isolator 10/16/2024

    By eliminating human intervention—the primary risk factor compromising drug sterility and quality—gloveless aseptic processing technology offers manufacturers greater flexibility, safety, and regulatory compliance in their filling operations.

  10. Vial Fogging: Practical Considerations For Vial Selection 10/16/2024

    Vial fogging is a common phenomenon observed in lyophilized biologic drug products. This document presents two case studies that explore critical factors contributing to vial fogging and inform vial selection decisions.