Pharmaceutical Dissolution Testing 2025
Modern Methods, Compliance, and Innovation in Drug Release Analysis
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Pharmaceutical Dissolution Testing 2025
Narrated by:
Virtual Voice
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Narrated by:
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Virtual Voice
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By:
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James Carter
This title uses virtual voice narration
Virtual voice is computer-generated narration for audiobooks.
About this listen
Dive into ten expertly crafted chapters that blend foundational knowledge with the latest 2025 advancements. Learn the fundamentals and regulatory requirements (USP, FDA, EMA, ICH, BCS), explore apparatuses and methods (basket to flow-through), and tackle media selection, validation, and troubleshooting with confidence. Discover how dissolution drives QC batch release, R&D formulation screening, and in vitro-in vivo correlation (IVIVC), while specialized sections cover complex forms like modified-release products, transdermals, and liposomes. Stay ahead with emerging trends—AI-powered profile prediction, real-time PAT tools, automation, 3D-printed drugs, and eco-friendly “green” dissolution—all distilled into practical insights. Wrap up with regulatory case studies and audit-ready strategies to ace inspections.
What sets this book apart? It’s comprehensive yet concise, packed with real-world examples, troubleshooting checklists, and appendices (glossary, SOPs, calibration schedules) that make it a go-to reference. Written by James Carter, a pharmaceutical veteran behind the acclaimed HPLC and UHPLC Unveiled, this guide offers unmatched expertise in a format that’s accessible to newcomers and seasoned pros alike. For a fraction of what you’d expect to invest in staying current, you get a front-row seat to the future of dissolution testing—without the jargon or fluff. Don’t miss out on this essential tool to elevate your skills, streamline your work, and ensure compliance in 2025 and beyond. Grab your copy now and see why it’s the smart choice for pharmaceutical professionals!
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