Do you know your PDE values?

Cleaning validation is a central element of quality assurance in the pharmaceutical industry. It ensures that residues of active ingredients, excipients, or cleaning agents are reliably removed and that cross-contamination is excluded. This seminar provides in-depth expertise on all aspects of cleaning validation in a GMP-regulated environment – from developing suitable cleaning procedures to establishing acceptance criteria, e.g., PDE values, to official evaluation.

In the workshop part, participants will work through practical examples to plan a risk analysis and define milestones in the validation process. The goal is to directly transfer the theoretical content to real operational questions.