Handling Failures in Sterile Manufacturing
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Date: 22nd - 23rd September, 2009
Location: Heidelberg, Germany
Summary:
Pharmaceutical - Seminar
Learning Objectives
You learn to systematically find deviations and failures in the manufacture of sterile medicinal products, to evaluate them and to handle them in a GMP-compliant way.
Case studies are used to demonstrate the evaluation and handling of real-life deviations and failures found in daily routine.
In workshops, you discuss and work out autonomous solution strategies for failures occurred in sterile manufacture.
You can discuss failures and deviations from your own daily practice with speakers and colleagues.