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Event Details
The U.S. FDA has announced the transition to V5 in their production environment. Given the significant changes included within this releaase, GlobalSubmit will provide a comprehenisve overview of the new features and functionality included within this release and implementation considerations to ensure successful deployment in your environment.
PRESENTER: Jason Rock, CTO GlobalSubmit, Inc.
AGENDA:
The agenda for this meeting is as follows:
- What’s New in V5?
- GlobalSubmit VALIDATE V5 Architecture
- Open V5 Demonstration
- Version 5.3 Sneak Preview
- GlobalSubmit’s Software Release Policy
- V5 Implementation Services - FastForward
- V5 Training Services
- Q&A
WHO SHOULD ATTEND:
This workshop is designed for all current subscribers and their teams responsible for the assembly, review, and validation of eCTD using GlobalSubmit software applications.
When & Where
Webcast Event
Conference Call,
19103
Tuesday, November 25, 2008 from 1:00 PM to 2:00 PM (ET)
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Hosted By
GlobalSubmit Announcement
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.
