Insights On Liquid Dose Manufacturing

1. Mitigating Risks In Sterile Injectable Manufacturing: How CMOs Can Ensure Product Safety 7/23/2025

   Sterile injectable manufacturing carries high risks. CMOs like Afton Scientific use rigorous quality systems, audits, and training to ensure patient safety, compliance, and product integrity.

2. How To Choose The Right Bowie-Dick Test Pack For Your Steam Sterilizer 11/26/2025

   Bowie-Dick testing is essential for compliance, but the choice between disposable and reusable systems impacts cost, waste, and efficiency. Learn how to balance sustainability with sterility assurance.

3. Barrel Filling Vs. Tip Filling A Syringe – Which Approach Should Be Used? 1/3/2025

   There are two primary filling methods for pre-filled syringes. Explore the pros and cons of each approach, highlighting why barrel filling is generally preferred in the pharmaceutical industry.

4. Engineering Challenges Of Designing Pharmaceutical Isolators 3/27/2025

   Designing pharmaceutical isolators requires navigating complex engineering hurdles, from ensuring chemical compatibility to optimizing airflow and pressure. Explore the critical considerations that guarantee drug manufacturing safety and efficiency.

5. Manufacturing Challenges With High Concentration Biologics 3/18/2024

   Explore key process operations, some of the challenges in manufacturing high-concentration biologics, and factors to consider for process optimization.

6. American-Made, Worldwide Benefit: Raising The Bar In Isolated Fill-Finish Manufacturing 3/18/2024

   Learn about the development process behind a new, state-of-the-art fill-finish isolator that's addressing issues in isolator manufacturing and servicing, as well as meeting the needs of the liquid pharmaceutical market.

7. Ready-To-Use Cartridges: Ensuring Compatibility For GLP-1-Based Drugs 8/27/2024

   Ready-to-use cartridges for GLP-1 applications offer safe, reliable self-administration. See how they can minimize complexities and better align with the stringent demands of modern manufacturing.

8. Navigating Your Holistic Approach To CCI For Biologic Drug Products 6/12/2024

   Explore regulatory framework and expectations, and see the benefit of a comprehensive approach to CCI tailored for mAbs and complex modalities such as fusion proteins or bioconjugates.

9. Isolator Air Handling: Advancements And Considerations For Fill-Finish Processing 3/28/2024

   When it come to fill-finish manufacturing of parenteral liquid pharmaceuticals, your choice of barrier technology is crucial.

10. Three Key Actions To Minimize Dead Volumes 10/10/2025

    Minimizing liquid dead volume helps labs conserve costly reagents and scarce samples while boosting assay throughput. Learn how advanced liquid level detection technologies are driving efficiency.