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Webinar: Global Regulatory Compliance for Aseptic Barrier Systems
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As global sterile manufacturing standards evolve, navigating differing expectations for isolators and RABS has become increasingly complex. In this webinar, ESCO experts compare FDA, EU GMP Annex 1, PIC/S, and WHO guidance, highlighting key differences in contamination control, documentation, monitoring, and validation. Attendees will gain practical strategies for designing and qualifying aseptic barrier systems that support globally compliant, inspection-ready manufacturing operations. Click here to learn more.
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Video | PTI Packaging and Inspection Systems
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Testing IV bags in compliance with Annex 1 guidelines requires a robust technology strategy to ensure product quality and patient safety. See how to deploy and validate technologies for IV bag CCI.
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Video | Adare Pharma Solutions
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Join Dr. Srinivasan Shanmugam to learn more about key strategies for selecting the right CDMO, reducing costs, accelerating timelines, and ensuring product success.
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Video | Stevanato Group
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Find tailor-made solutions designed to deliver high-quality standards even when scaling up. Modularity enhances production efficiency, saves costs, and shortens time to market.
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Video | West Pharmaceutical Services, Inc.
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Gain insight into an innovative system that delivers an integrated, verified solution designed to streamline submissions, support reliable supply, and reduce development risk.
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Video | Pharmaceutical Online
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In this segment from the Pharmaceutical Online Live event, “Proactive Contamination Control in Aseptic Fill-Finish,” our panelists talk about equipment vs. operator intervention, reducing intervention with better design, and the use of automation and robotics to reduce intervention.
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Video | Siemens
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Module Type Package enables plug‑and‑produce manufacturing through standardized interfaces. It simplifies integration, reduces engineering effort, and helps manufacturers reconfigure production.
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