Blend Uniformity in Pharmaceutical Solid Dosage Forms

The objective of this study is to explore the understanding of Blend Uniformity in the manufacture of solid oral dosage forms under current Good Manufacturing Practices (cGMP). For many years particle size has been recognized as a key parameter in the development and manufacture of a wide range of pharmaceutical materials and is routinely measured and controlled at many different stages of research, development, manufacture and quality control. This article highlights the importance and development of blend uniformity.

Click here
it read entire article