pharm-stream-recent-webinars

  1. Advancing Topical Formulations With Innovative Preclinical Models 11/17/2025

    A robust formulation development approach integrates scientific principles, systematic formulation development, and preclinical models to facilitate early identification of candidates with poor developability.

  2. Accelerate Your pDNA And mRNA Process Development 11/13/2025

    Explore a structured approach to optimizing and scaling plasmid DNA production using E. coli, with insights into key growth parameters, benchtop feasibility, and pilot-scale performance.

  3. Driving Robust Tech Transfer In Biologics: Computational Fluid Dynamics (CFD) Simulation 11/12/2025

    Computational Fluid Dynamics simulation is essential for robust biologics tech transfer. See how this predictive tool optimizes critical scale-up processes, reducing risk and expediting time to market.

  4. Practical Solutions For Protein Analytics And Residual DNA Testing 11/12/2025

    Discover practical solutions for common quality control bottlenecks in biotherapy manufacturing. Learn how to improve protein analytics and DNA testing robustness and accelerate time to market.

  5. Choosing The Right Sporicide: Critical Factors For Robust Cleanroom Contamination Control 11/10/2025

    Choosing the best sporicide for your cleanroom involves evaluating factors like surface format, contact time, and safety. Learn the criteria to select an effective and robust agent for contamination control.

  6. Driving Sustainability In Bioprocessing With Biobased Single-Use Solutions 11/7/2025

    Discover how biobased materials in bioprocessing enable measurable carbon emission reductions. Learn practical strategies to meet decarbonization goals and adopt greener, operationally sound practices.

  7. Achieve Pharma 4.0 With Next Generation Software-Defined Manufacturing 11/5/2025

    Explore how software-defined manufacturing is helping companies overcome legacy system challenges, improve OEE by up to 25%, and accelerate batch release cycles while maintaining compliance.

  8. Enhancing Viral Vector Sterile Filtration: Process Efficiency And GMP Alignment 11/4/2025

    Explore filtration strategies that improve viral vector yield and quality, with insights on AAV and lentivirus workflows, plus practical guidance for implementing PUPSIT in line with requirements.

  9. Innovations, Solutions, And USP <1062> With Scale Up 11/4/2025

    Optimize tablet compression by simplifying calibration, speeding up changeovers, and utilizing advanced laser inspection to prevent critical punch tip wear and maintain quality.

  10. Faster Tech Transfers Through Seamless Digital Transformation 10/30/2025

    Manual process documentation slows innovation. Learn how modular libraries and digital connectivity enable faster, error-resistant execution, bridging the gap between process design and automation.