About this document
IP Guidelines for Dissolution Testing by monikaola is a document available to read on EtoBox.
Dissolution testing is an important quality control procedure performed on pharmaceutical dosage forms to evaluate drug release and bioavailability. There are several USP and unofficial dissolution testing apparatus that use different agitation mechanisms and conditions. The test measures the rate and extent of dissolution of the drug substance from the dosage form under specified conditions of pH, temperature, agitation etc. Dissolution testing is necessary for batch-to-batch consistency evaluation, produc
- Author
- monikaola
- Language
- EN