Insights On Liquid Dose Manufacturing
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How DFM Promotes Scalability, Repeatability, And Profitability
6/28/2024
Find out why it is critical that OEMs see and understand the benefits of taking time to build a mold or create automation more robustly to achieve long-term savings and higher annual production.
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Innovation For Subcutaneous Delivery Of Large-Volume Complex Biologics
5/9/2024
Explore the key findings of a new wearable injector clinical trial, including its positive impact on patient experience and the broader benefits of wearable injectors for chronic disease management.
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What Does Annex 1 Mean For Cryovial Filling?
10/6/2025
New sterile manufacturing rules require major changes to cryovial filling. Ensure compliance by adopting better "first-air" protection, minimizing human contact, and using 100% dose checks.
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Filling Syringes With Spray-Dried Powders - The How, The Why And The Benefits
11/3/2025
Discover how filling spray-dried powders directly into syringes improves stability, minimizes cold chain reliance, and accelerates administration speeds for critical therapies.
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Sterility Testing Media And Rinse Fluids Manufactured In A Center Of Excellence
6/4/2024
MilliporeSigma’s Center of Excellence in France focuses on producing sterility testing products for the pharmaceutical industry to ensure that patients worldwide are administered microbiologically safe drugs.
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Still Pipette-Filling Cryovials? There's A Better Way
7/7/2025
Manual cryovial filling in cell therapy is risky, time-consuming, and unsustainable. Learn why automating this crucial step is essential for precision, viability, and scalability.
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5 Common Bowie-Dick Test Failures And How To Prevent Them
11/26/2025
Bowie-Dick test failures indicate serious sterilization issues. Learn the five most common causes and proven strategies to prevent downtime, compliance risks, and compromised product integrity.
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A Direct Path To Annex 1 Compliance With Blow/Fill/Seal Technologies
9/13/2025
Learn how Blow/Fill/Seal technology supports contamination control, reduces operator risk, and meets sterility assurance requirements under dynamic conditions with advanced airflow and monitoring.
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Fill And Finish: Your Final Step Is Our First Priority
12/9/2025
Fill and finish demands precision, compliance, and adaptability. Learn how flexible solutions and expert support can help you overcome complexity, reduce risk, and ensure quality in this final step.
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Optimizing Aseptic Processing With Isolator Technology
9/29/2025
Discover how pharmaceutical isolators optimize operations, achieve higher sterility assurance, and meet stringent regulatory requirements. Learn about design principles, validation, and VHP cycles.