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Event Details
For those of you who weren't able to sign up for the November 5th event, or have colleagues that didn't hear about it in time, we're holding another webinar on December 8th!
If you:
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Don’t have time to keep up-to-date on eCTD regulations and guidance around the world
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Are Wondering when eCTD will become mandatory, or even accepted, in a given market?
Join GlobalSubmit and CATO Research on Tuesday, December 8th at 11:00 AM EST for a free educational webinar titled, eCTD Regulations and Status Worldwide.
Industry expert Kathie Clark will review the status of eCTD in the US, Europe, Canada, Japan, Australia and Switzerland. Clark, creator of the eCTD Summit blog, will also summarize guidance and present the latest updates for each region. As well, Kathie will provide you with a convenient list of references and contacts.
At the end of the session’s Q&A, a CATO representative will give a brief overview of the latest happenings in the CRO realm and answer any questions you may have.
Date: December 8, 2009
Time: 11:00 AM EST -- This time is European friendly!
Note: Dial-in/Logon information will be sent to you on December 7th. Please note that this event is designed for sponsors and not for consultants, vendors or other third parties. You must register with an email address from a valid pharmaceutical domain to attend.
When & Where
Webcast
Philadelphia,
PA 19103
Tuesday, December 8, 2009 from 11:00 AM to 12:00 PM (ET)
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Hosted By
GlobalSubmit Product 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 leads international efforts, comprising industry and government agencies, to standardize product and study information. The company is headquartered in Philadelphia, Pennsylvania.