GLOSSARY: Dissolution Testing

Dissolution Testing is defined as a critical formulation tool in the process of drug discovery that entails measuring the stability of the investigational product, achieving uniformity in production lots and determining its in vivo availability. The Dissolution Testing method is useful in the pharmaceutical and biotechnology industry to formulate drug dosage forms and to develop quality control specifications for its manufacturing process. What are the 7 Deadly Sins of Quality Assurance and Quality Control? Find out here www.pharmaqualitytraining.com