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Interested in expanding your knowledge of Good Automated Manufacturing Practice (GAMP), Computerized System Validation, Regulations, and more? Experts from QbD Group will be instructing a 2-day training that will do exactly that.

This 1-day course focusses on giving a thorough introduction to pharmaceutical freeze drying.

The Sustainable Systems Engineering (STEN) group offers a comprehensive training on Sustainability and Life Cycle Assessment (LCA), providing a solid foundation in sustainability assessment methods and LCA applications within the pharmaceutical industry.

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.

The Efficient Data Processing training is a hands-on course designed to help participants accelerate their data workflows.

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 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.