USP applies metrological principles to the dissolution procedure alone and in collaborative studies to understand and minimize potential sources of variability. According to the International ...

When it comes to dissolution testing, research is focusing on ways to extend its reach, improve in-vitro and in-vivo correlation, and make real-time release testing a reality. Studying how a drug ...

In addition to use of dissolution testers, this three-day course will also cover equipment qualification, development and validation of dissolution procedures, and the use of dissolution testing in ...

Explore how you can continue to use Apparatus 1 and 2 effectively to meet today’s testing needs despite these new formulation complexities. USP Dissolution Apparatus 1 and 2 have been used since the ...

The dissolution profile of inhaled drugs underpins therapeutic efficacy and is an area of increasing regulatory scrutiny, particularly for the demonstration of bioequivalence in a generic. The new ...

that would penetrate the first stage of the impactor), the ex-throat dose or the Fine Particle Dose (FPD); the fraction of the dose defined as respirable on the basis of size. The dose is collected on ...