Insights On Liquid Dose Manufacturing

  1. 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.

  2. SEDDS: Improving Oral Bioavailability Of Poorly Soluble Compounds 8/20/2026

    Nearly 90% of marketed drugs have poor water solubility. Learn how self-emulsifying drug delivery systems (SEDDS) resolve oral bioavailability failures across BCS Class II and IV compounds.

  3. The Journey Of A CDMO Choosing Pre-Sterilized Drug Containers 2/4/2025

    Explore innovation in pharmaceutical manufacturing with advanced drug containment, delivery systems, and automation, ensuring quality, safety, and efficiency in injectable therapies for global healthcare.

     

  4. 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.

  5. Ensuring Integrity: Testing Viscous Biologics In Pre-Filled Syringes 12/18/2025

    Viscous biologics in pre-filled syringes demand precise integrity testing. Discover how advanced HVLD technology detects micro-defects and ensures sterility, meeting stringent USP <1207> standards.

  6. CDMO Uses Robotic Gloveless Isolator For Advanced Therapeutics 4/28/2025

    CDMOs must innovate production architectures to meet the demands of advanced therapeutics to ensure a reliable supply and compliance. Discover how these approaches advance modern medicine and improve patient outcomes.

  7. Efficient, Single-Source PFS Supply 5/21/2026

    When component lead times don’t align, inventory piles up, cash gets tied up, and forecasts can quickly turn into waste or shortages. What if a single integrated PFS system could simplify it all?

  8. Design Verification Done Right: Smarter Strategies For Prefillable Syringes 9/29/2026

    A practical framework for planning and justifying design verification programs for prefillable syringes, covering test selection, acceptance criteria, and sample-size rationale within a risk-based approach.

  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. Validating VH2O2 Decontamination Cycles For Product And Personnel Safety 6/30/2026

    Discover how ultra-sensitive spectroscopy transforms decontamination validation, revealing hidden efficiencies that safely cut facility downtime while ensuring absolute safety.