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.
The Investigational Medicinal Product Dossier (IMPD): EU CTA vs. FDA IND: Comparing the Content and Agency Expectations - Webinar By GlobalCompliancePanel
21 June 2012, Wilmington,DE, United States
Introduction
Venue
Online Training
Online Training, 1000 N West Street, DE, Suite 1200, Wilmington,DE, 19801, United States
Useful links
Organised by
GlobalCompliancePanel
Contact information
Related events
TAC 2025 - 60th Anniversary Conference
14 April 2025 09:00 - 16 April 2025 17:00, Guildford, United Kingdom
What's in that Perfume? - The Chemistry behind an iconic Christmas gift
3 December 2024 18:00-20:00, London, United Kingdom
Chemistry Teaching in Practice
9 January 2025 09:30-16:00, Oxford, United Kingdom
Joint SoBRA / 澳门六合彩开奖记录 Winter Conference 2024 Current Issues in Contaminated Land Risk Assessment
10 December 2024 09:45-18:00, London, United Kingdom
Search
Advertisement
Spotlight
Explore
Membership
