Insights On Liquid Dose Manufacturing

  1. Meet Regulation Requirements With RTU Vials And Cartridges 10/9/2025

    Sterile manufacturing remains vital, with resilient supply chains preventing shortages. Industry and regulators prioritize integrity as demand surges, making it the fastest-growing pharmaceutical segment.

  2. Still Pipette-Filling Cryovials? There's A Better Way 7/7/2025

    Manual cryovial filling in cell therapy is risky, time-consuming, and unsustainable. Learn why automating this crucial step is essential for precision, viability, and scalability.

  3. Thermo Fisher Scientific Large Volume Liquid Expansion 5/2/2024

    Take an insightful look into the expansion of the large volume liquids manufacturing site at the Grand Island facility, highlighting the various stages of the manufacturing process and the capabilities it offers to support the bioprocessing industry.

  4. Importance Of Assessing Mannitol Crystallinity In Lyophilized Drug Products 10/16/2024

    Drug product stability may be seriously compromised if mannitol completes crystallization during storage rather than during the freezing or annealing step in the lyophilization process.

  5. Enable Low Volume Delivery Of Proteins In Aqueous Solutions 11/7/2025

    Achieve ultra-low volume dispensing of proteins and aqueous solutions without surfactants with consistent precision, minimal contamination, and broad compatibility to streamline your lab workflow.

  6. Future ATMP Manufacturing Paradigms, Part 2 3/28/2025

    Discover how AI, Industry 4.0, and innovative drug containers are transforming the future of Advanced Therapy Medicinal Product (ATMP) manufacturing for better patient outcomes.

  7. Does Blow/Fill/Seal Aseptic Packaging Make Sense for Your Drug? 7/2/2024

    Watch to learn about patent-pending Annex 1 technologies and the versatility of drug products that can be filled with Blow/Fill/Seal systems

  8. Scaling Personalized Medicines For Flexible Aseptic Filling 2/14/2024

    Traditional aseptic filling solutions can introduce contamination and variability. Learn about Cytiva's commitment to finding innovative solutions and improving patient outcomes in the field of medicine.

  9. The Successful Implementation Of A New Aseptic Filling Line 10/10/2024

    Discover how a Quality by Design approach can streamline the development of new sterile product filling lines, featuring a real-life example illustrating its effectiveness.

  10. Sterility Method Development And Suitability Testing 6/4/2024

    Does each formulation and product type require method development? Explore a matrix approach to method development and suitability testing for the compounding industry.