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The Qualified Person and other technical/managerial personnel need to be informed and aware of pharmaceutical legislation. Changes in legislation and guidelines, and the interpretation of them, can have significant implications for the individual and their company.This is the continuation of a very successful series of one day seminars that are designed to form part of your Continuing Professional Development. What You Will Learn: The reality and interpretation of recent and new EU legislation - Changes to EU GMPs - An update on ICH and other international initiatives - USA changes to legislation and FDA guidance - UK updates.