On-Demand Fill/Finish Webinars

  1. The Future Of Cell Therapy Development And Delivery 10/6/2023

    Experts discuss the latest strategies for navigating the complexities of cell therapy development and identify clinical development best practices for a successful execution.

  2. Theory Of DSC And Applications In Lyophilization Processes 5/5/2023

    In this episode, Austin Ryan, Ph.D., reviews how DSC works and provides background on the MDSC technique, what it does, and how it can be useful in lyophilization applications.

  3. Future-Proof Your Aseptic Filling 2/24/2023

    Using the Cytiva SA25 Aseptic Filling Workcell, a standardized system designed with flexibility built in, ensures that companies can pivot between products quickly and adapt as manufacturing needs change.

  4. Single-Use Final Filtration Process Design Considerations 6/6/2022

    We describe the major considerations when establishing a single-use final filtration step, and show how new product design features can be used to help meet regulatory expectations.

  5. Understanding The Impact Of Osmolality Within Formulation 5/26/2022

    This webinar focuses on the role osmolality plays in developing formulations as new drug classes and compositions are being investigated.

  6. Moving The Needle: A Final Filling Case Study Webinar 5/20/2022

    Watch this webinar to hear about a collaboration that helped optimize their new filling line with single-use needles and reduced downtime.

  7. Implementing Single-Use Technologies In Formulation And Filling Of Vaccines 3/25/2021

    Formulation and filling is a critical part of any drug manufacturing process and demands the highest levels of quality and reliability. Pall has a range of technologies and services that enables end users to carry out their operations with increased reliability and flexibility – while ensuring the product quality is designed into the manufacturing process. Using technology from the Allegro™ single-use portfolio, Pall sterilizing grade filters and Pall’s automated solutions ensure that manual interventions are minimized and increased sterility assurance is achieved.

  8. Orphan Drugs: Balancing Financial Incentives & Complex Challenges

    Whether your orphan drug is a small or large molecule, there are key strategies to enable a seamless transition from early development into commercial manufacturing, while also balancing your investment.

  9. Survival Kit For Quality Regulations: A Closer Look At Lyo Packaging

    Explore primary packaging developed following well-established ICH principles for sustainable compliance and vial container closure systems for product development and commercial manufacturing needs.

  10. Key Considerations When Outsourcing An Aseptic Fill/Finish Project To A CMO Partner

    This presentation addresses keys to outsourced drug production, including the importance of seeking the right partnerships to help overcome the challenges associated with secure commercial product supply.