September 27, 2016 Princeton, New Jersey: Navitas Life Sciences releases paper on CDISC, the standards and why the upcoming December 18th FDA deadline matters
The FDA (and eventually, regulatory agencies from around the world) will require clinical data sent to them to be in CDISC standards. Georgina Wood, Navitas’ Clinical Data practice leader writes about CDISC, the various standards and what it all means for the industry.
click here to download the whitepaper.
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