Pharmaceutical Online Videos

31. The Body As A Bioreactor – Delivering The Vision 8/8/2026

    Making the body a bioreactor requires precise delivery to selected cells. See how lipid nanoparticles, manufacturing science, and biology are converging to overcome biological barriers and improve the targeting of advanced therapies.

32. Resilience Capabilities Update July 2026: Fill/Finish 8/7/2026

    Learn how expanding capacity, automation, and flexible manufacturing technologies are helping biologics manufacturers meet evolving market and quality demands.

33. FUJIFILM Biotechnologies Capabilities Update July 2026: Gene Therapy 8/7/2026

    From process development to GMP manufacturing, our teams operate as one connected system to support your cell or gene therapy through every milestone.

34. Supporting Digital Documentation With AI 8/6/2026

    In this segment from the Pharmaceutical Online Live event, “Building Inspection Ready Systems With Digital Documentation,” panelists talk about how the AI layer fits in to support verification and validation as well as trending the data, but address what guardrails are needed, including human oversight in data review. They also address what happens if AI misses something.

35. Clear Data Handoffs And Cross-functional Teams 8/6/2026

    In this segment from the Pharmaceutical Online Live event, “Building Inspection Ready Systems With Digital Documentation,” panelists talk about maintaining clean data handoffs when there are multiple platforms involved to avoid gaps in accountability. They also discuss how cross-functional teams can better support regulatory compliance.

36. Real-Time Deviation Management 8/6/2026

    In this segment from the Pharmaceutical Online Live event, “Building Inspection Ready Systems With Digital Documentation,” panelists discuss deviation management, CAPA and root cause analysis change when documentation becomes real-time and data driven.

37. Paper To Digital Transition And Paper Fallback 8/6/2026

    In this segment from the Pharmaceutical Online Live event, “Building Inspection Ready Systems With Digital Documentation,” experts discuss common compliance gaps when transitioning from paper-based or hybrid documentation systems to digital systems, including: incomplete system validation, poorly defined user requirements, training and, change management. The panelists also discuss the mindset that may be holding them back from transitioning and where it is important to have a paper fallback.

38. Changing Inspection Readiness Into Continuous Improvement 8/6/2026

    In this segment from the Pharmaceutical Online Live event, “Building Inspection Ready Systems With Digital Documentation” our panelists talk about transitioning from the old approach of preparing for an inspection to continuously being ready for the inspection, including how leaders can get their team on board.

39. SK Pharmteco Capabilities Update July 2026: Gene Therapy 8/3/2026

    Adaptive viral vector platforms pair scalable manufacturing with targeted purification. Customizing workflows ensures high vector purity and cost efficiency, accelerating clinical development.

40. Andelyn Capabilities Update July 2026: Gene Therapy 8/3/2026

    Modular vector platforms blend custom transfection with gentle purification. Optimized TFF plus precise chromatography yield high vector recovery across diverse cell and gene therapy applications.