Insights On Liquid Dose Manufacturing

  1. 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.

  2. A Risk-Based Decision Framework For Selecting Aseptic Barrier Technologies 3/20/2026

    EU GMP Annex 1 requires a risk-based approach to selecting Isolators or RABS. This framework evaluates human intervention and decontamination to ensure robust sterility assurance.

  3. Biofluorescent Particle Counters Are Gaining Momentum 4/28/2025

    The 2025 BioPhorum report highlights challenges and trends in drug filling operations and how they are advancing towards biofluorescent particle counters. Discover an approach that aligns with industry needs.

  4. Gain Speed To GMP Filling 2/24/2025

    Discover the advantages of a filling technology that provides faster readiness to good manufacturing practices (GMP) filling compared with traditional options.

  5. Protecting Your Drug Product 5/13/2026

    With patient lives depending on every dose, even minor vulnerabilities in containment or delivery systems can have serious consequences for product integrity and patient outcomes.

  6. 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.

  7. Navigating The New USP Chapter <382> For Elastomeric Closures 6/24/2025

    Dive into the scope of <382> for pharmaceutical closures and the regulatory landscape, which includes new required tests, instrumentation for compliance, and recommendations on implementation.

  8. A Brief History Of Aseptic Processing 3/27/2025

    From Bunsen burners to advanced isolators, aseptic processing has evolved significantly. Delve into the evolution of this crucial manufacturing method, from its early sterilization techniques to today's highly controlled and regulated environments.

  9. 5 Ways Pre-Filled Syringes Contribute To Better Patient Outcomes 5/23/2025

    In our series on pre-filled syringes, we explore five key ways this delivery format is enhancing patient outcomes, not just through the medicine it contains, but through the device design itself.

  10. AST Origins: Pioneering RTU Flexibility With Robotic Fill-Finish Systems 3/25/2026

    Modernize sterile manufacturing with robotic fill-finish systems. Achieve multi-format flexibility and risk reduction to meet the rigorous demands of personalized medicine and small-batch production.