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Free Webinar - Standardizing Powder Flow Characterization in Pharma: Ensuring Compliance & Efficiency - April 15, 2025 from 4 to 5 PM (CET)
Achieving consistency in pharmaceutical manufacturing starts with standardized powder flow characterization. Join us on April 15, 2025, for an insightful webinar where we will explore how precise and repeatable powder flow measurements enhance efficiency and regulatory compliance.
Why Attend?
In pharmaceutical processes such as formulation, blending, tableting, and capsule filling, powder flow properties play a crucial role in ensuring product quality and process efficiency. Standardized and automated characterization methods help reduce variability, minimize operator influence, and align with key industry regulations such as:
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USP 1174 – Flow Through an Orifice & Angle of Repose
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USP 616 – Bulk Density and Tapped Density of Powders
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GMP, PAT, and 21 CFR Part 11 compliance
What You Will Learn
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How GranuFlow, GranuHeap, and GranuPack provide automated and repeatable powder flow measurements
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The impact of angle of repose, tapped density, and flowability on pharmaceutical production
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Real-world case studies demonstrating the benefits of standardization
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How to enhance quality control, process efficiency, and regulatory compliance
Who Should Attend?
This webinar is designed for pharmaceutical scientists, process engineers, quality control specialists, and R&D professionals looking to optimize powder handling and manufacturing processes.
Don’t miss this opportunity to gain valuable insights and practical data on improving your pharmaceutical processes.
Speaker: Giuseppe Rosario Del Sorbo, Ph.D., Sales Manager at Granutools
Date: April 15, 2025