Our courses

The DOE training is hands-on and designed for individuals who want to actively engage in Experimental Design and gain a better understanding of the statistical analysis of experimental data.

To support both innovation and efficiency in pharmaceutical development, manufacturing, and quality assurance, the FDA proposed its process analytical technology or PAT framework (2004).

This course focusses on giving a thorough introduction about the tableting process in an interactive manner.

This 2-day course focusses on giving a thorough introduction on pharmaceutical freeze-drying.

This course is divided into two separate modules:

This course aims to show the wide range of relevant material characterization methods which were widely used in the development of the UGent raw material database and published articles.

This 2-day course focusses on giving a thorough introduction on twin screw processing. Two different aspects will be covered: twin screw wet granulation and hot melt granulation.

This course addresses the question of how we can keep pharmaceutical processes in optimal manufacturing conditions while ensuring versatility, resilience and quality of end product.