Obtaining User-Defined Particle Size Distribution Using Dry Granulation
By Dejan Djuric
Publication
Article
Pharmaceutical TechnologyPharmaceutical Technology-04-15-2014
Volume 2014 eBook
Issue 1
The author examines the effect of compaction force, gap width, and sieve setup on granule size.
Users can define a desired particle-size distribution using continuous dry granulation. The author examines the effect of compaction force, gap width, and sieve setup on granule size.
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Pharmaceutical Technology’s 2014 Solid Dosage and Excipients eBook.
Articles in this issue
Safety by Design—Mitigating the Risk of Medication Errors Through Product Design
Controlled-Release Technologies Create Opportunities for Solid-Dosage Drug Formulators
Continuous Manufacturing for Solid-Dosage Drug Production
A Practical Guide to Hot-Melt Extrusion Scale-Up for Pharmaceutical Applications
Using Modular Systems in Solid-Dosage Manufacturing
Advances in Hot-Melt Extrusion Manufacturing
Obtaining User-Defined Particle Size Distribution Using Dry Granulation
A Quality-by-Design Approach to Optimize In-Process Curing of EUDRAGIT NM 30 D
Selection of Excipients in Generic Formulations
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