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If you work in pharmaceutical industry, you will sooner or later be faced with health authority meetings, be it during product development, during the application for a marketing authorisation or later in the lifecycle of your drug to discuss pharmacovigilance matters.
This important course covers Health Authority (HA) meetings and other interactions in the EU and the US. You will learn by performing role plays, and through many case studies.
This course is a hands-on course full of practical work. It is necessary that you bring your laptop with you.