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.
Optimizing Semisolid Dosage Forms
Dec 02, 2015
By Agnes Shanley
Pharmaceutical Technology
Volume 39, Issue 12
By Agnes Shanley
Pharmaceutical Technology
Volume 39, Issue 12