Insights On Liquid Dose Manufacturing

31. Benefits Of Isolator Technology In Fill-Finish 12/10/2025

    Isolator technology enhances sterility assurance, reduces contamination risk, improves operator safety, and supports regulatory compliance, making it essential for modern aseptic fill-finish operations.

32. Barrel Filling Vs. Tip Filling A Syringe – Which Approach Should Be Used? 1/3/2025

    There are two primary filling methods for pre-filled syringes. Explore the pros and cons of each approach, highlighting why barrel filling is generally preferred in the pharmaceutical industry.

33. Advancing Moisture Determination Of Pharmaceutical Products 10/10/2025

    Learn how water activity testing offers a more predictive, non-destructive alternative to traditional moisture analysis, with insights into USP <922>, lyophilized products, and rapid headspace techniques.

34. 5 Key Questions On Implementing Pharma 4.0™ Solutions For Fill-Finish 12/1/2025

    Pharma 4.0 leverages IoT, AI, and automation to enhance drug quality. Evaluate your fill-finish line readiness by considering five key questions on modularity, high-risk process automation, and data integration.

35. EU GMP-Annex 1: Changes, Challenges, And Ready-To-Use Sterile Packaging 8/27/2024

    Leveraging a pre-sterilized containment solution that meets the requirements of Annex 1 and outsources non-core activities can help prevent contamination and reduce the effort and liability of the CCS.

36. American-Made, Worldwide Benefit: Raising The Bar In Isolated Fill-Finish Manufacturing 3/18/2024

    Learn about the development process behind a new, state-of-the-art fill-finish isolator that's addressing issues in isolator manufacturing and servicing, as well as meeting the needs of the liquid pharmaceutical market.

37. Visual Inspection Equipment To Deliver The Highest Product Integrity 4/1/2025

    Gain insight into an advanced inspection solution for pharmaceuticals that ensures drug integrity and reduces costs with flexible technologies, from lab development to high-volume production.

38. Lifecycle Planning For Containment And Delivery Of Biologics Drug Products 6/20/2024

    Read more about trends in the biologics market that could impact the lifecycle strategies for your drug product and steps you can take around drug packaging early in development.

39. Optimizing Aliquoting For Robust Cell And Gene Therapy Processes 6/3/2024

    Explore the challenges of liquid handling in cell and gene therapy processes as well as innovative solutions to simplify aliquoting in modern bioprocesses.

40. Contamination Control Strategies: Comparing Cleanrooms, RABS, Isolators 10/20/2025

    Sterile manufacturing relies on three main contamination control strategies (CCSs): cleanrooms, RABS, and isolators. Understand how each system compares in sterility assurance, startup cost, and operational flexibility.