Contact GlobalSubmit Announcement for event and ticket information.
Thursday, November 05, 2009 from 2:00 PM - 3:00 PM (ET)
Don’t have time to keep up-to-date on eCTD regulations and guidance around the world?
Wondering when eCTD will become mandatory, or even accepted, in a given market?
Join GlobalSubmit and CATO Research on Thursday, November 5th at 2:00 PM 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: November 5, 2009
Time: 2:00 PM EST
Note: Dial-in/Logon information will be sent to you shortly after you register.
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.
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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