Optimizing Semisolid Dosage Forms

Quality by design, in-vitro release testing, and modern analytical methods are improving understanding and control of these complex formulations.

Years ago, when excipients were called “fillers” or “inactive ingredients,” drug-product quality testing was simple. The traditional approach, however, often sets the stage for process variability and manufacturing and quality problems.

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Optimizing Semisolid Dosage Forms
Dec 02, 2015


By Agnes Shanley
Pharmaceutical Technology
Volume 39, Issue 12
305075-page=full.pdf
Adobe Acrobat Document 200.1 KB