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The two-day process validation in the US and EU, balancing science and risk during the product lifecycle meeting will help you gain an understanding of the EU and FDA process validation guidance, learn how to establish a process validation programme, under the link between Quality by Design and process validation as well as how to apply relevant tools for process validation including risk assessment.
Benefits of attending:
Know the scope of the FDA and EU validation guidelines
Establish a three-stage, science and risk-based, lifecycle process validation programme
Clarify similarities and differences between EU and US expectations
Understand how Quality by Design supports process validation
Realise significant business benefits from taking a science and risk-based approach
