Insights On Liquid Dose Manufacturing
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Consistent, Reliable, High-Quality Components
2/3/2026
Discover a premium line of components for vials, prefilled syringes, and cartridge systems developed and refined to provide best-in-class levels of quality, performance, and risk mitigation.
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What To Consider When Looking For A CDMO In Drug Substance Utilization
6/17/2026
Optimize drug substance use during fill/finish. Learn how advanced line configurations and 100% non-destructive weight checks mitigate process drift, protect therapeutics, and prevent product loss.
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Enzyme Indicator Technology
5/13/2026
Watch this video to learn how enzyme indicators provide real-time, quantitative data to optimize bio-decontamination and accelerate validation.
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From API Synthesis To Drug Product Shelf Life
8/20/2026
Fragmented drug development causes delays and added costs. Unifying API synthesis, fill-finish, and testing streamlines logistics, preserves product data, and accelerates regulatory timelines.
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A Standardized Gloveless Robotic Isolator
10/16/2024
By eliminating human intervention—the primary risk factor compromising drug sterility and quality—gloveless aseptic processing technology offers manufacturers greater flexibility, safety, and regulatory compliance in their filling operations.
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Enhancing Biopharmaceutical Production Through Advanced Mixing
6/30/2026
Eliminate particulate contamination and product degradation in downstream bioprocessing. Learn how frictionless, levitating impeller technology ensures low-shear mixing and high yields.
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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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EZ-fillĀ® Kit: RTU Packaging Solutions For Fast Access To Small Volumes
2/4/2025
Discover the EZfill Kit in action—an innovative solution designed to streamline and enhance precision in liquid handling, optimizing efficiency for pharmaceutical and bioprocess applications.
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Generate CHO-K1 GFP-Expressing Cells For Cell Line Development Workflow
11/7/2025
Discover a high-efficiency workflow for generating GFP-expressing CHO-K1 clones using automated single-cell dispensing to achieve 93% isolation success and stable expression in under five weeks.
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Rethinking Fill-Finish To Reduce API Loss In Early Development
6/15/2026
Early-stage drug programs can preserve constrained API supplies by replacing large-scale manufacturing defaults with deliberate, right-sized fill-finish designs that minimize avoidable process waste.