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| Successfully Navigating Opportunities With On-Body Delivery Systems – Common Questions And Answers | Container Closure Integrity (CCI) is essential to ensure sterile drug products remain safe, effective, and contamination-free throughout their shelf life. USP <1207> recommends evaluating package integrity from development through commercialization by defining the Maximum Allowable Leakage Limit (MALL) and selecting validated, application-specific test methods. The guidance favors quantitative deterministic methods over probabilistic approaches and emphasizes integrating CCI testing, seal quality assessment, stability studies, and lifecycle management to maintain product quality. |
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By Hiep X. Nguyen, DPharm, Ph.D., DTM, California Northstate University | Let's take a closer look at the scientific principles, technological progress, and translational hurdles defining the present state of microneedle research. | |
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| The Hidden Costs Of Multiple-Vendor Contract Manufacturing | Article | Pharma & MedTech Partner Division, B. Braun Medical Inc. | When it comes to outsourcing in medical device manufacturing, learn more about these consequences and present the advantages of working with a single-source contract manufacturer. |
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| How Fluids Impact Variable Volume Pump Performance | Article | The Lee Company | Explore the factors influencing variable volume pump performance, from fluid viscosity and temperature to chemical compatibility and flow stability, ensuring reliable operation and system longevity. |
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| Design Freedom Before Steel | Article | Accumold | Micro 3D printing helps OEMs validate designs, reduce risk, and accelerate development before tooling, enabling more confident decisions and smoother transitions to production. |
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