Insights On Liquid Dose Manufacturing
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Minimizing Particulate Risk
5/13/2026
While visible particles often draw immediate attention, visual inspection alone is insufficient, as subvisible particulate matter can pose equally significant risks to patient safety.
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Low Temperature Storage Containment For Vial And Syringe Systems
6/20/2025
With the growth of advanced therapy medicinal products, there is an increased need for specialized low-temperature packaging solutions, particularly for vials and syringe systems at -50°C to ≤ -130°C.
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Ensure Sterility In Small-Batch Drug Production
1/9/2026
Automation and sterility are critical for small-batch drug manufacturing. Learn how robotic isolators streamline vial filling, reduce contamination risk, and support advanced therapies with precision.
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Navigating Sterile Injectable CMO Selection: A Technical And Quality Assessment
6/11/2025
Learn how to carry out an effective technical and quality assessment and what specific criteria to prioritize when selecting a sterile injectable CMO partner.
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Simplify Cell Line Development
11/7/2025
A streamlined workflow combining microfluidic dispensing and multimodal imaging enables efficient single-cell isolation, viability assessment, and outgrowth analysis to support cell line development.
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Syntegon Virtual Pharma Expo May 2025: Aseptic Manufacturing And Packaging
5/21/2025
The 2022 EU GMP Annex 1 revision marks a pivotal shift in sterile manufacturing, emphasizing contamination control, advanced technologies, and global harmonization—driving industry-wide adaptation and regulatory interpretation challenges.
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5 Key Questions On Implementing Pharma 4.0 Solutions For Fill-Finish
12/1/2025
Pharma 4.0™ leverages IoT, AI, and automation to enhance drug quality. Evaluate your fill-finish line readiness by considering five key questions on modularity, high-risk process automation, and data integration.
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CDMO Checklist To Choose The Right Aseptic Isolator
1/9/2026
Selecting the right isolator for aseptic filling requires more than comparing features. Discover essential questions to ask and make informed decisions that align with your process and operational goals.
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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.
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A Simple Method For Cell Growth Media Preparation
11/3/2025
Explore how powder media and sterile fluid handling can reduce contamination risk and improve efficiency in viral vector production, especially for HEK293-based AAV workflows.