Insights On Liquid Dose Manufacturing

31. Fluid Management Strategies For Scalable Biopharmaceutical Production 4/16/2025

    Effective fluid management systems are indispensable in therapeutic manufacturing. Discover how modular design, automation, and single-use systems enhance scalability and maintain product integrity.

32. Navigating Sterile Injectable CMO Selection: A Technical And Quality Assessment 6/11/2025

    Learn how to carry out an effective technical and quality assessment and what specific criteria to prioritize when selecting a sterile injectable CMO partner.

33. From Batch, To Continuous Chemistry, To Continuous Processing 5/14/2024

    Explore how understanding the transport phenomenon in the boundary layer can allow us to engineer the flow to manage the rate-limiting step and intensify the process.

34. Compressed Gas Contamination: Guidelines For Control In Aseptic Manufacturing 10/18/2024

    Explore key guidelines for preserving the purity and quality of compressed gas, with an emphasis on contaminants, monitoring, and preventive maintenance practices.

35. Enhancing Aseptic Fill-Finish Processes 7/3/2025

    Achieve exceptional product recovery and sterility. Learn about high-integrity surge bags, advanced leak detection, and flexible design options for your fill-finish applications.

36. 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.

37. Step Into The Future Of ATMP Fill-Finish 5/21/2025

    Discover the future of ATMP manufacturing as Josh Russell from AST demonstrates an advanced, fully automated fill-finish system featuring automated bag and tub opening, as well as the Atmos isolator.

38. Compressed Gas Systems In Aseptic Manufacturing 10/18/2024

    Learn about compressed gas systems and why effectively identifying and managing the risks associated with these systems is critical for maintaining product quality and ensuring compliance with GMP.

39. Isolated GENiSYS C Fill-Finish System: Available For Quick Delivery 1/17/2025

    Accelerate your parenteral drug production with a fully integrated, isolator-based fill-finish system. Compact design, rapid delivery, and maximum yield for agile drug development.

40. Automated Production Line For Vial Filling And Crimping – A Case Study 4/16/2025

    Discover how a leading pharmaceutical manufacturer overcame space constraints and regulatory requirements to increase vial filling and crimping capacity through a custom-designed automated system.