GlobalSubmit's 2008 Executive Webinar Series: Mastering the eCTD - Working With Metadata

Developing and assembling an eCTD requires a working knowledge of practical techniques associated with metadata.  This seminar will review the submission metadata required by ICH, FDA and other agency specifications, discuss the impact it has on the submission outline (such as repeating of sections), and summarize the decisions that need to be made concerning metadata.  If you are involved in the preparation and assembly of the eCTD, you will not want to miss this briefing.

Wednesday, October 22, 2008 from 11:00 AM - 12:00 PM (ET)

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GlobalSubmit

GlobalSubmit is THE eCTD Company. Our mission is to promote the adoption, implementation, and quality of global submissions based on the eCTD format. GlobalSubmit's flagship applications, GlobalSubmit REVIEW and GlobalSubmit VALIDATE are used exclusively by leading global life sciences organizations and exclusively by the U.S. FDA. GlobalSubmit also offers services, complimentary to its applications, to accelerate implementation. These services include eCTD readiness, electronic assembly and publishing, regulatory content management, eCTD pilot programs, and much more.

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