New research shows that magnesium and other metals in mine waste can be solubilized and recovered thanks to acid-producing bacteria. Researcher Nathan van Wyk believes that the method has great ...
Dissolution is a common characterization test used by the pharmaceutical industry to guide formulation design and to control product quality. It is often a required performance test for solid dosage ...
As the pace of product development accelerates, the approach to dissolution-method development must advance beyond a manual method and an assay. A natural progression of the method-development process ...
DUBLIN--(BUSINESS WIRE)--The "Troubleshooting Dissolution Methods for Solid Oral Dosage Forms" webinar has been added to ResearchAndMarkets.com's offering. By attending this webinar, you will learn ...
This 8-hr webinar on Dissolution Methods for pharmaceutical dosage forms will provide you a comprehensive understanding of the development process and present a systematic approach for dissolution ...
The Joint Pharmaceutical Analysis Group, JPAG, is proud to present the Pharmaceutical Analysis Foundations Programme. A series of 1 day events designed to provide in-depth guidance on the most ...
Liquid mixing scale-up in pharmaceutical industry has often been based on empirical approach in spite of tremendous understanding of liquid mixing scale-up in engineering fields. Propylparaben was ...
When you take a time-release drug, you count on it doing what the package says: release the drug slowly into your bloodstream to provide benefits over the specified period of time. When the drug ...
Pharmaceutical dissolution testing for solid oral dosage forms is a complex analytical procedure where the control of critical variables (environmental conditions, equipment performance, sample ...
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