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Event Details
SUBMIT WITH CONFIDENCE!
Delivering quality submissions to global regulatory agencies can be a daunting task without the right tools to help you succeed. GlobalSubmit cordinally invites you to attend our FREE open demonstration of our eCTD application suite designed to help organizations review and validate submissions based on the eCTD format. Our applications are used across the globe by leading life sciences companies and exclusively by the U.S. Food and Drug Administration on the desktops of over 300 reviewers.
Who Should Attend:
This webinar should be attended by all stakeholders responsible for the review and validation of regulatory submissions including regulatory affairs/operations personnel, I.T. professionals, electronic submission publishers, document control, quality assurance, and other professionals responsible for the assembly and publishing of the eCTD.
What You Will Learn:
- eCTD Assembly and Publishing Challenges
- How To Effectively Review and Validate Your eCTD
- eCTD Study Tagging File Best Practices
- Validation Error Checks and Conditions
- Comprehensive Validation Review Processes
- Submission Lifecycle Management
- eCTD Readiness
- Perspectives on RPS
- ... and much more!
REGISTER TODAY!
When & Where
Webcast Event
Conference Call,
19103
Tuesday, December 2, 2008 from 10:00 AM to 11:00 AM (CT)
Add to my calendar
Hosted By
GlobalSubmit Demonstration Team
GlobalSubmit is a products and services company that provides transparency in regulated healthcare products. The U.S. Food & Drug Administration and leading Life Sciences companies use our flagship applications, REVIEW™ and VALIDATE™, to review and validate electronic submissions. GlobalSubmit’s thought leaders lead international efforts, constantly working with industry and government agencies to standardize product and study information. The company is headquartered in Philadelphia, Pennsylvania.
