Enterprise Solutions Webinars

  1. Expanding The OSD Toolbox 10/3/2024

    This session is designed to provide practical solutions for enhancing bioavailability and scalability in pharmaceutical formulations.

  2. Understanding Nitrosamines: Key Regulations And Best Practices 10/2/2024

    Gain expert insights into nitrosamine regulations and discover practical strategies for ensuring compliance and safeguarding product safety.

  3. Understanding FDA Calibration Requirements And Best Practices For Reducing Risks 10/2/2024

    Become equipped with the tools and strategies needed to strengthen your calibration efforts and better position your organization for success in regulatory audits.

  4. What Do You Need To Qualify A Single-Use Assembly? 10/2/2024

    Explore best practices for the qualification of single-use systems, focusing on quality and regulatory documentation.

  5. Extractables And Leachables: Setting Up Early For Success With Your CDMO 10/2/2024

    Discover insights tailored specifically for drug product researchers and manufacturers, offering key knowledge on extractables, leachables, and effective implementation strategies.

  6. Strategic Antibody Outsourcing: Guidance On Selection, Services, And Facility Fit 9/24/2024

    How do you choose the best CDMO for your program? In this presentation, experts share insights and best practices on selecting, qualifying, and managing CDMO partnerships.

  7. MicroCNX® Series Connectors: Introducing The MicroCNX ULT And MicroCNX Luer 9/23/2024

    Experience the future of connectivity. Designed for enhanced simplicity and productivity, these innovative connectors are perfect for cell therapies requiring cryogenic freezing and sterile connections.

  8. Formulation And Process Development For High-Concentration Subcutaneous Biologics Drug Product 9/20/2024

    Delve into the specific challenges encountered in the development of high-concentration formulations and gain an overview of current state-of-the-art solutions for subcutaneous administration.

  9. Navigating Challenges In Biologics Process Development And Characterization 9/18/2024

    Delve into the key obstacles encountered in biologics process development, including the complexities of optimizing production processes, ensuring product consistency, and maintaining quality control.

  10. Manufacture To Control: Considerations In CMC For Antibody-Drug Conjugates 9/18/2024

    The complex nature of ADCs necessitates meticulous attention to CMC. Gain valuable insights for navigating CMC development, ensuring the delivery of safe and efficacious biopharmaceutical products.