Insights On Liquid Dose Manufacturing

  1. Sterility Method Development And Suitability Testing 6/4/2024

    Does each formulation and product type require method development? Explore a matrix approach to method development and suitability testing for the compounding industry.

  2. Water For Injection: Strategic Utility And The Case For Outsourcing 3/9/2026

    Water for Injection is a critical, highly regulated component of sterile drug manufacturing. Outsourcing its production offers faster timelines, reduced risk, and improved operational and cost efficiency.

  3. 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.

  4. CDMO Checklist To Choose The Right Aseptic Isolator 1/9/2026

    Selecting the right isolator for aseptic filling requires more than comparing features. Discover essential questions to ask and make informed decisions that align with your process and operational goals.

  5. 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.

  6. 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.

  7. Effective Strategies To Minimize Product Loss During Fill Finish 5/11/2026

    Every drop of high-value biologic lost in fill finish is money left on the table. Learn practical strategies to protect your yield.

  8. 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.

  9. 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.

  10. 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.