Outsourced Pharma Webinars

  1. Mastering The Complexities Of Gene Therapy Document Writing 5/20/2025

    Gain the insight and strategic flexibility needed to confidently navigate the unique scientific, regulatory, and documentation challenges of gene therapy development.

  2. Solving The AOC Puzzle: Strategies For Chemistry, Manufacturing, And Regulatory Success 5/20/2025

    Gain valuable insights from industry experts on overcoming the unique chemical, technical, and regulatory challenges of AOC development by watching the recorded webinar.

  3. Optimizing Biotherapeutic Protein Expression With CHO Vector Technology 5/19/2025

    Review the development of a high-strength synthetic gene promoter that enhances titers while maintaining exceptional product quality and expression stability, to support more efficient biomanufacturing.

  4. Combination Products: Navigating Regulatory Strategy, Design Verification 5/19/2025

    Delve into the intricacies of combination products and the regulatory expectations, including risk-based determination, evaluation, and documentation approaches for performance requirements.

  5. Utilizing A Stepwise Approach For Nitrosamine Risk Mitigation 5/15/2025

    The following insights and case studies demonstrate how a tailored, stepwise testing approach can effectively detect, quantify, and control nitrosamine impurities while maintaining cost efficiency.

  6. Digital Transformation In Contract Manufacturing: A Leadership Perspective 5/13/2025

    Discover how PCI Pharma Services embraced digital transformation and gain expert insight on overcoming challenges, driving innovation, and maintaining core values in a regulated industry.

  7. Little Patients, Big Challenges: Developing Pediatric Formulations 5/12/2025

    Explore the development of high-quality, child-friendly oral formulations, as well as learn about new testing requirements for impurities and innovative approaches to creating age-appropriate medications.

  8. The Importance Of Cognitive And Pharmacodynamic Testing During FIH Trials 5/9/2025

    Learn how to identify which cognitive and pharmacodynamic tests are required for novel CNS-active drugs and best practices on conducting them during First-In-Human (FIH) trials.

  9. PUPSIT Without The Pain: Practical Solutions For Implementation 5/6/2025

    Explore the critical role of pre-use post-sterilization integrity testing in quality risk management, as well as learn about integrity testing, wetting procedures, and innovative filtration systems for effective implementation.

  10. CLD To Upstream Optimization: Enhancing Biologics Quality, Productivity 4/30/2025

    Explore how advanced cell line development and upstream processing strategies optimize both productivity and therapeutic effectiveness, ensuring the development of high-quality biologics.