Thermo Fisher Bioproduction Insights

  1. Leveraging 3 Distinct Resins To Provide Effective Impurity Removal For mAbs And Novel Antibody Derivatives 11/3/2025

    Due to the complexity of bispecifics, Fc-fusion proteins, and Fab fragments, their manufacturing poses added purification challenges and requires a robust toolkit of purification techniques.

  2. Considerations For Buffer Preparation As You Grow 10/29/2025

    Buffer preparation strategies impact cost, efficiency, and risk. This infographic compares in-house vs. outsourced approaches, helping teams align supply decisions with growth, operational needs, and long-term production goals.

  3. How To Mitigate Particulate Contamination In cGMP 10/28/2025

    Maintaining cGMP standards, controlling particulate contamination ensures drug safety, quality, effectiveness, and shelf life while preventing immune reactions and regulatory noncompliance.

  4. How Can You Avoid Bioprocessing Risks When Using Cable Ties? 10/15/2025

    Cable ties in bioprocessing can cause leaks, damage, and delays. See how switching to a uniform-sealing connector can significantly improve efficiency, reduce prep time, and minimize contamination risks.

  5. Simplify Process Scale-Up With An Innovative Single-Use Bioreactor 10/15/2025

    Consistent cell growth and protein yields from 5 L to 5,000 L show how a unified bioreactor design can simplify scale-up, reduce risk, and accelerate upstream process development in bioproduction.

  6. Advanced Aseptic Filling Assembly Helium Integrity Testing 10/15/2025

    Helium leak testing offers unmatched sensitivity for detecting micro-leaks in single-use fill-finish systems. Learn how tighter leak thresholds can strengthen aseptic processing and regulatory confidence.

  7. Product Recovery Study For Fill Finish Applications 10/15/2025

    Surge bags are essential to fill finish efficiency, but poor drainage can cause costly product loss. Learn how drainage testing helps identify high-performance bags that maximize recovery and reduce waste.

  8. How To Overcome Common Single-Use Assembly Design Challenges 10/15/2025

    Single-use systems offer major benefits in pharma manufacturing, but design complexity brings challenges. Learn how to overcome issues like scalability and quality assurance with integrated strategies.

  9. Molecular Approaches To Streamline Cell Therapy Product Analytical Testing 9/26/2025

    Learn how rapid molecular methods of cell therapy testing like qPCR for mycoplasma, sterility, and lentiviral quantification are key to accelerating product release and timely treatment delivery.

  10. Advances In Analytical Method Selection And Technology Transfer 9/26/2025

    Successful analytical method transfer is crucial for product quality and regulatory compliance. Learn best practices for tech transfer, including how gap assessments mitigate common risks and streamline bioprocessing.