Liquid Dose Filling

  1. Mycap® Bottle Closures – Aseptic Fluid Transfer Systems For Bottles 9/6/2022

    The innovative MYCAP bottle closure system provides more options for aseptic fluid transfer in bottles and rigid containers. The elastomeric closure makes it a truly universal closure system.

  2. 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.

  3. Streamline Your Path To Clinical Fill 5/21/2026

    Drug-independent PFS testing is a required early step — but it can be time-consuming and resource-intensive. What if you could eliminate the effort without losing the data you need?

  4. A Data-Driven Approach To Container Closure Integrity

    Gain confidence in your container closure system selection by utilizing a stepwise and data-driven approach to predicting and verifying container closure integrity.

  5. Quality Time With Oliver: Guest - Andy Goll 10/5/2026

    Blow-fill-seal technology enables custom single-dose liquid packaging for surgical applications, accommodating viscous liquids, emulsions, and suspensions that standard formats cannot handle.

  6. Solutions In Pre-Filled Syringes For Biologics And Ophthalmic Applications 6/19/2025

    Discover how pharma companies can select tailored pre-filled syringes for biologics and biosimilars by aligning drug delivery needs with specialized containers and analytical services.

  7. Early-Stage Considerations For The Selection Of Pre-Fillable Syringes When Developing A Vaccine 5/14/2021

    Get an overview of the strategy to speed up the migration from a vial to a pre-fillable syringe. Explore the main considerations in meeting and overcoming PFS-drug challenges when developing a vaccine.

  8. Driving Excellence In Aseptic Fill-Finish: A Strategic Partnership With Stäubli Robotics 5/29/2025

    See how intelligent automation and purpose-built robotics deliver contamination control and operational excellence in demanding sterile manufacturing environments.

  9. EU Med Device Regulations: Ensuring Compliance For Integral Combination Products

    Review the EU Medical Device Regulation (MDR) changes, specifically with respect to integral combination products, and examine the technical documentation packages supporting functionality and content.