Description
The formulation and processing conditions employed in the manufacture of medicinal and biological products have a significant effect upon their safety, quality and efficacy. Even apparently minor changes to the incoming materials and/or processing conditions can have a significant effect on content uniformity, stability, bioavailability, and other critical quality attributes which are not detectable by routine Quality Control testing. The Qualified Person (QP) must understand all aspects of pharmaceutical manufacture.
Module deliveries for 2024/25 academic year
Last updated
This module description was last updated on 8th April 2024.
Ìý