Insights On Manufacturing Logistics
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Planning For Scale-Up
5/21/2026
From rapid early-stage production to scalable commercialization, discover the packaging and continuity challenges companies face as they prepare for launch.
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Understanding The Regulatory Landscape For Ophthalmic Drug Products
5/14/2026
Learn how evolving ophthalmic regulations, contamination control strategies, and advanced packaging solutions can help support compliance, product quality, and patient safety.
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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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Protecting Your Drug Product
5/13/2026
With patient lives depending on every dose, even minor vulnerabilities in containment or delivery systems can have serious consequences for product integrity and patient outcomes.
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Establishing A Container Closure System
5/13/2026
As a trusted partner to both established and emerging drug developers, we support the safe, effective containment and delivery of life-saving and life-enhancing medicines.
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Start Packaging Development Early
5/12/2026
To avoid costly delays later in the product lifecycle, it is essential to plan for key variables early and select container closure systems with confidence from the outset.
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USP Draft Chapters On CCS: What You Need To Know
5/12/2026
Learn why it's important to stay aligned with evolving Annex 1 expectations to support sterility assurance, regulatory compliance, and patient safety across sterile drug manufacturing operations.
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USP <788> Revisions And Why Packaging Matters More Than Ever
5/12/2026
Prepare for the upcoming USP <788> revisions by strengthening your particulate control strategy to support regulatory compliance, product quality, and patient safety across injectable drug products.
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Why Lower Endotoxin Levels Matter: Raising The Bar For Patient Safety And Product Quality
5/12/2026
Strengthen patient safety and regulatory compliance with comprehensive endotoxin control strategies designed to support the evolving demands of injectable and advanced pharmaceutical products.
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Annex 1 FAQs: Responding To The 2022 Revision
5/11/2026
Viewing the Annex 1 revision as a natural extension of current habits, rather than a burden, allowed for a seamless transition. Since contamination control was already standard, the update simply validated existing excellence.