This webinar will provide the new and expected guidances on data standards and electronic submissions for drugs and medical products. We will explain what are the policies and the requirements for submissions and standards for drugs in US and globally and how it affects healthcare/drug industry to adopt them.
e-Submissions & Data Standards for FDA (eCTD, CDISC, HL7) - Webinar By GlobalCompliancePanel
25 April 2013, Fremont, United States
Introduction
Venue
Online Training
Livermore Common, Online Training, California, Fremont, 94539, United States
Useful links
Organised by
GlobalCompliancePanel
Contact information
Mr John Robinson
Livermore Common, Fremont, 94539, United States of America
8004479407
Contact us by email
Livermore Common, Fremont, 94539, United States of America
8004479407
Contact us by email
Related events
7th International Conference on Nanomaterials Science and Mechanical Engineering
8 July 2025 08:00 - 11 July 2025 18:00, Aveiro, Portugal
Drugging the Multimorbidity Associated with Ageing
17 January 2025 09:30-17:00, London, United Kingdom
Future Labs Live Basel
27 May 2025 09:00 - 28 May 2025 17:00, Basel, Switzerland
European Glycoscience Community Webinar Series
25 January 2024 15:00 - 19 December 2024 18:00
Search
Advertisement
Spotlight
Explore
Membership
