Biologic Videos

  1. WuXia TrueSite 5/19/2026

    Targeted integration adds predictability to cell line development by cutting clone screening, improving expression consistency, and accelerating timelines to ease early CMC bottlenecks.

  2. Built for Performance: High‑Quality Cartridge Production 5/19/2026

    A focused look at automated 3 mL cartridge processing, from washing and sterilization to monitored aseptic filling. Learn how precision filling, oRABS, and automation enable consistent, compliant production.

  3. How To Advance Self-Administered Therapies 5/18/2026

    Scale your biologic fill-finish from vials to autoinjectors without disruption. See how integrated device assembly capabilities support every clinical phase through commercialization.

  4. Evaluating The Entire Package System Under USP 382 5/18/2026

    USP 382 introduces holistic packaging evaluation, focusing on container closure integrity, functionality, and real-world conditions to ensure sterility, safety, and product reliability.

  5. Strategic Early Material Generation For Accelerated Process Development 5/14/2026

    Learn how early material generation strategies can accelerate biologics development, streamline process optimization, and enable scalable, production-relevant material supply from the earliest stages of development.

  6. Optimizing Outcomes In ADC Manufacturing 5/13/2026

    As bioconjugates evolve, optimized conjugation and strong process and analytical strategies are essential for ensuring consistent quality, targeted characteristics, and reliable therapeutic performance.

  7. ADC Outsourcing: Plan Smart Now Or Suffer Later 5/11/2026

    Antibody-drug conjugates (ADCs) bring together multiple scientific and operational disciplines, which makes early and ongoing outsourcing decisions especially consequential. This event examines how sponsors think through outsourcing strategies across discovery support, process development, bioconjugation, analytical work, drug substance, and fill-finish, focusing on what should remain internal and what should be outsourced to external partners.

  8. Design Scalable Downstream Processes With Practical Strategies 5/11/2026

    Downstream purification is becoming more complex as new modalities enter development. Learn how advanced analytics and chromatography strategies can support scalable, confident process development.

  9. Annex 1 FAQs: Responding To The 2022 Revision 5/11/2026

    Viewing the Annex 1 revision as a natural extension of current habits, rather than a burden, allowed for a seamless transition. Since contamination control was already standard, the update simply validated existing excellence.

  10. Annex 1 FAQs: Why Is A Good Supplier Partnership Pivotal To Meet Regulatory Expectations? 5/11/2026

    Struggling to keep pace with EU GMP Annex 1? The right supplier partnership brings critical regulatory insight your team may be missing. Learn how strategic collaboration closes compliance gaps and prepares you for future regulations.