The Ultimate Cheat Sheet on CDISC-SEND

Chris Lovejoy

On December 18, 2016, numerous regulatory agencies will require electronic submission of non-clinical data using CDISC’s standard format. What exactly are CDISC data standards and how will they impact drug developers? In this blog post, I will provide an overview of the CDISC SEND data standard, review some of the requirements for implementing SEND, and […]

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Topics: Model-based Drug Development, PK/PD Modeling and Simulation
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