Avantor Featured Articles

  1. Overcoming Scale-Up Challenges In Viral Vector TFF 10/29/2025

    Discover how a tailored TFF solution delivers a scalable, high-yield process that integrates smoothly with existing infrastructure and maintains regulatory compliance.

  2. Implementing A Versatile Mixing System To Drive Down Costs 10/29/2025

    Learn how a CDMO reduced capital expenses and operational complexity by adopting an all-in-one mixing solution that supports every stage of production and a wide range of volumes.

  3. A Strategic Assessment Tool For Modernizing Buffer Preparation In Biologics Facilities 8/14/2025

    Modern biomanufacturing requires a strategic, multi-criteria approach to buffer management. Discover how a hybrid model can optimize your operations and address fluctuating demands.

  4. Minimizing Fluid Loss By Monitoring Back Pressure During Clarification 6/12/2025

    Learn how a biopharma manufacturer mitigated the significant financial risk of fluid loss with a pressure-sensing pump that now protects their high-value product during clarification operations.

  5. Scaling Up Viral Vector Harvest With Ease And Regulatory Compliance 4/11/2025

    Explore how scalable, high-performance solutions can help you overcome the challenges of large-volume viral vector production and accelerate the delivery of life-changing gene therapies.

  6. Peristaltic Pump Configuration Saves Days Of Production Time 11/14/2024

    Explore how a molecular biology client improved their fill-finish efficiency by configuring a peristaltic pump, reducing fill time, minimizing agitation, and saving significant technician time annually.

  7. Advancing Clinical Trials Manufacturing From Pilot To Production 10/16/2024

    Scaling manufacturing of clinical trial materials requires careful planning to ensure flexibility and compliance with quality standards. Explore essential strategies to advance production and sample management.

  8. Pre-Use Post Sterilization Integrity Testing (PUPSIT) 10/8/2024

    Explore how, when, and why pre-use post sterilization integrity testing (PUPSIT) should be used and how to navigate the complexities of filter integrity testing.

  9. Overcoming Efficiency And Quality Challenges In Gene Therapy Development 10/8/2024

    Review the importance of collaboration and innovation in addressing the challenges with scaling up gene therapy production, from adopting new cell lines to integrating AI in process optimization.

  10. Key Drivers To Overcome Obstacles In mAbs Formulation And Fill-Finish 7/11/2024

    Discover the key strategies to overcome, aided by comprehensive support from suppliers, to streamline the formulation and fill-finish process and deliver effective mAb therapies on time.