LSC Recent Webinars on BIO

  1. Sterile Gas Filtration And Optimization In Bioprocessing 4/17/2025

    Unlock insights into sterile gas filtration challenges in bioprocessing. Watch this on-demand session to learn optimization strategies for critical applications and improved filter performance.

  2. Navigating Global Regulatory Landscapes In An Evolving Biopharma Industry 4/15/2025

    Minimize regulatory risks and ensure compliance in the evolving biopharma sector. Watch this on-demand discussion for insights on change management, supplier collaboration, and future market trends.

  3. Transforming Rare Disease Drug Development For A Faster Cure 4/15/2025

    This comprehensive exploration aims to shed light on the critical aspects of expediting curative therapies, with a focus on the strategic role that CDMOs can play in this transformative journey.

  4. Optimize Your Process For Producing High-Concentration Drugs 4/10/2025

    Explore the challenges and solutions in high-concentration monoclonal antibody manufacturing, which includes practical strategies for maximizing product recovery and optimizing processes for efficient production.

  5. Optimal Tech For Predicting Drug Responses At The Cellular Level 4/1/2025

    Explore how preserving spatial molecular information and leveraging AI-driven spatial-omics can transform treatment prediction, patient stratification, and personalized medicine.

  6. Minimizing Risk In RNA-LNP Encapsulation And Drug Product Manufacturing 3/31/2025

    Learn about an integrated drug substance/drug product offering for your IND program and beyond, with a holistic approach to ensure process robustness at every stage.

  7. Adapting To Evolving Regulations: Validation In A Changing Landscape 3/26/2025

    Discover how evolving regulatory expectations in life sciences present new challenges and opportunities, as well as gain insight into strategies from experts in the field to navigate risk-based validation processes.

  8. Do Not Bear Cross Contamination In The Pharmaceutical Industry – Prevent It 3/25/2025

    Learn how thorough cleaning and process optimization in pharma manufacturing prevent cross-contamination, ensure product integrity, and enhance efficiency while also improving compliance and reducing costs.

  9. Shifting Drug Development With Advanced Analytical Characterization 3/24/2025

    Explore the advancing mass spectrometry, biophysical characterization, automated sample preparation, and high throughput analytics required to deliver medicines in a safe, compliant, and efficient manner.

  10. Clinical-Grade Manufacturing Of Difficult-To-Transduce Cells 3/20/2025

    Discover how Miltenyi R&D and Bioindustry experts revolutionize cellular therapy with BaEV-env LVVs as well as gain insights into preclinical evaluations and clinical-grade product development for CAR-NK cells.