Q&A

An Inside Look About The CDISC Standards Required For FDA Submissions

Source: ClinCapture

Carey Smoak is the co-founder and co-leader of the CDISC Device team. He has authored and co-authored more than 30 papers on the topic and has done numerous presentations at PharmaSUG, SAS Global Forum, the Bay Area SAS Users Group, the Bay Area CDISC Implementation Network, and other venues. Carey Smoak has a master’s degree in public health and currently works for Portola Pharmaceuticals as a Director of Statistical Programming.

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