Provides dissolution test conditions and a helpful search function in a downloadable database.

For hard or soft gelatin capsules and gel- atin-coated tablets that do not conform to the Dissolution specification, repeat the test as follows.

1. Why do some USP Monographs have multiple dissolution / drug release / disintegration tests? performance tests for products that were approved by FDA to be marketed in the United States. …

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 fashion.

Nov 24, 2015 · This free searchable database contains the test conditions (except Tolerance and Acceptance Criteria) as stated in the sections referring to dissolution, disintegration or drug Release …

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

This test is provided to determine whether tablets, capsules, or granules USP 1-Aug-2019 disintegrate within the prescribed time when placed in a liquid medium at the experimental conditions presented …

US Pharmacopeia (USP)

As moisture can impact the dissolution results in the Performance Verification Test (PVT), remaining tablets from an opened sachet should not be saved for later use.

The USP Performance Verification Test (PVT) assesses the suitable performance of apparatus used in dissolution testing. This assures reliability of dissolution results that reflects the quality of the drug …