The United States Pharmacopeia emphasizes mechanical calibration and a performance test to esnure integrity of the dissolution procedure. The intent of the USP performance verification test (PVT), ...
This webinar will provide participants with an understanding of USP and FDA requirements for dissolution instrument qualification and provide strategies that will enhance success and minimize resource ...
Industry, equipment vendors, and regulators are busy refining the precision and reliability of dissolution testing. Solid dosage formulators rely on dissolution testing to mechanically model the ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback