Insights On Liquid Dose Manufacturing

  1. Low Temperature Storage Containment For Vial And Syringe Systems 6/20/2025

    With the growth of advanced therapy medicinal products, there is an increased need for specialized low-temperature packaging solutions, particularly for vials and syringe systems at -50°C to ≤ -130°C.

  2. Cutting Through Complexity: An Integrated Model For Faster PFS Development 4/7/2026

    Discover how integrated, end-to-end development for prefilled syringes can streamline timelines, enhance patient-centric delivery, and scale efficiently from early development to global launch.

  3. Product-Wet Integrity Testing: Risk-Based Strategies 5/22/2026

    When standard water‑based integrity testing falls short, product‑wet approaches can offer a more representative alternative. Learn how risk‑based strategies are used to establish reliable test limits.

  4. A State-Of-The-Art Syringe Liquid Sampler 6/24/2025

    Discover a cutting-edge syringe liquid sampler for Life Sciences that offers USP <788> compliance, versatile syringe compatibility, and advanced features for precise particulate testing.

  5. Selecting A Prefillable Syringe System With Confidence 2/5/2026

    Discover an advancement in the prefillable syringe market, uniquely integrating the syringe barrel, plunger, and needle shield/tip cap into a fully harmonized, verified system from a single supplier.

  6. How Do We Reduce Your Environmental Cost Of Ownership (ECO)? 12/4/2025

    By rethinking cleanroom requirements and reducing resource-heavy sterilization steps, manufacturers can significantly lower their Environmental Cost of Ownership and futureproof their operations.

  7. 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.

  8. Building A Science- And Risk-Based Bio-Decontamination Strategy 10/5/2026

    Annex 1 has made bio-decontamination central to sterility assurance, with isolator and barrier cycles now expected to be designed, justified, and reviewed across their lifecycle.

  9. Powering The Next Generation Of Drug Delivery Systems 12/4/2025

    Discover how pharmaceutical extrusion, including aseptic methods, enables advanced drug delivery systems, detailing the critical process controls required for success with complex and novel drug products.

  10. Ensure Stability And Safety Of Your Vaccine Formulations 7/2/2026

    Optimize vaccine production with integrated manufacturing, analytical testing, containment solutions, and automated inspection for efficient, reliable scale-up.