Insights On Liquid Dose Manufacturing

  1. Expanding The Viscosity Limits Of Peristaltic Dosing 12/17/2025

    Discover how innovations in closed-loop control and mechanical design extend peristaltic dosing limits to 2000 cP, maintaining accuracy while preserving the advantages of sterile, disposable paths.

  2. Delivering On GLP-1 Demand: Combining Device And Supply Strategy 5/7/2024

    Meeting the demand for GLP-1 treatments requires robust and efficient delivery systems. Review how innovative solutions offer customization, streamlined manufacturing, and formulation compatibility.

  3. Shaping The Future Of ATMPs: Tailored Automation And Advanced Technologies For The Next Decade 3/27/2025

    From personalized treatments to large-scale viral vector production, the future of ATMPs hinges on optimized automation. We delve into the technologies driving this transformation and the challenges ahead.

  4. Commercially Proven Sterile Fill/Finish With Capacity And Global Backing 1/27/2026

    Find comprehensive solution with new sterile fill/finish investments supporting complex molecules through robust tech transfer, commercialization expertise, and integrated cGMP manufacturing solutions.

  5. Advanced Isolator Tech Boosts Manufacturing Efficiency And Quality 7/30/2024

    Isolator technology can run continuously over several days, minimizing operator interaction and other opportunities to introduce contamination — ideal for high-volume, time-limited production runs.

  6. Demystifying Lyophilization: Understanding The Freeze-Drying Process 5/23/2024

    Advancements in lyophilization technology and research have helped overcome inherent challenges and ensure the safety and efficacy of lyophilized pharmaceuticals.

  7. Accelerating The Industrialization Of CGT Manufacturing 5/1/2025

    Patent expiry of original product enables 3P innovation to design enhanced equivalent DPI filling system for developers and CMOs.

  8. Maintaining Sterility Through Precise Component Design And Manufacture 2/4/2026

    Prioritizing high-quality component design and manufacturing excellence can mitigate risks, ensure long-term container closure integrity, and avoid the costly delays associated with non-compliance.

  9. Consistent, Reliable, High-Quality Components 2/3/2026

    Discover a premium line of components for vials, prefilled syringes, and cartridge systems developed and refined to provide best-in-class levels of quality, performance, and risk mitigation.

  10. Isolators For Pharmacy Compounding – Time For Change? 3/14/2025

    Maintaining a contamination-free environment is crucial in drug compounding. Learn how isolator systems can improve safety, efficiency, and regulatory compliance.