Toronto, Canada (PRWEB) June 21, 2013
Last year’s renewal of the Prescription Drug User Fee Act indicates that the FDA will require all submissions to include the clinical data in a standard format, within approximately 3 years. This standard is assumed to be the Study Data Tabulation Model (SDTM) maintained by CDISC.
Join us for an exciting webinar, led by experts from OmniComm and Alkermes, on strategies for incorporating SDTM in all your studies.
This webinar will:
To learn more about the event, visit: http://xtalks.com/SDTM-in-Real-Time.ashx.
Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars to the global Life Sciences community. Every year thousands of industry practitioners turn to Xtalks for access to quality content. Xtalks helps Life Science professionals stay current with industry developments, trends and regulations. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.
To learn more about Xtalks visit http://xtalks.com/ContactUs.ashx.
Karen Lim (416) 977-6555 ext 227
Read the full story at http://www.prweb.com/releases/2013/6/prweb10852093.htm.
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