A dissolution test uses an apparatus with specific test conditions in combination with acceptance criteria to evaluate the performance of the product. General chapter <711> Dissolution …

The determination of suitability of a test assembly to per- form dissolution testing must include conformance to the dimensions and tolerances of the apparatus as given above.

The purpose of these videos is to provide a detailed description of the best practices associated with the Mechanical Qualification and Performance Verification Test (PVT) for the USP basket …

See below for answers to questions about dissolution test apparatus, performance verification testing, and protocols—sinkers, peak vessels, mini paddles, mesh size and more.

Scope: This document provides a description of best practices associated with the mechanical calibration and performance verification test for the USP basket and paddle dissolution …

Get information about the USP Performance Verification Test (PVT), performance verification reference standards, PVT acceptance criteria and dissolution assemblies.

Learn more about the USP dissolution test and how it plays a role in evaluating the performance of a drug product (article) and indicating when the drug product performs in a substandard …

The USP Performance Verification Test (PVT) is an integral part of the General Chapter Dissolution and assesses proper dissolution apparatus performance.

Nov 24, 2015 · Users can easily find out what monographs specify use of a specific apparatus, which methods require mediums with a certain pH value, where the preparation of a particular …

3. How will USP process my submission for a new dissolution / drug release /disintegration test? If the test is a part of a new monograph submission, a complete monograph proposal will be …