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Introduction

This 90 minute training course will provide your company the opportunity for comprehensive understanding of the IMPD (Investigational Medicinal Product Dossier) and the structure and content differences between a EU CTA Application and an FDA IND Application. Additionally, this webinar covers many related processes sponsors will need to know, as they file for, conduct and close-out effective clinical studies in the U.S. and EU.

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Venue

1000 N West Street | Suite 1200

1000 N West Street | Suite 1200, 1000 N West Street, DE, Suite 1200, Wilmington, 19801, United States

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Organised by

GlobalCompliancePanel

Contact information

Mr webinars web
Online Training, 1000 N West Street, Suite 1200, Wilmington, 19801, United States of America
8004479407
Contact us by email

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