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Mark Wheeldon (Formedix) and Paula McHale (PAREXEL Informatics) discuss available tools and standards to reduce the time and cost of an end-to-end clinical trial, in this webinar recording.
Watch our recent learning webinar as Mark Wheeldon and Kevin Burges discuss optimizing both new and legacy studies using CDISC standards.
Get the presentation from the Formedix learning webinar about optimizing new and legacy studies using CDISC.
This infographic illustrates six of the most common challenges that CROs experience in the battle to win sponsor business.
Download the slides from Formedix CEO Mark Wheeldon's presentation at the New Jersey CDISC User Group in Merck, Summit, discussing all things CDASH.
Hear how Formedix and Medidata have partnered to implement CDISC together across the entire end-to-end clinical trial process, in this webinar recording.
Mark Wheeldon (Formedix) and Joshua Pines (Medidata) team up to talk all about end-to-end clinical trial automation using CDISC, in this presentation.
This presentation discusses real life-experiences of using CDISC Database Standards (Operational Data Model) to drive efficiencies in study setup and study build.
Presentation from Formedix-hosted Bay Area Executive Breakfast, discussing standards to enable efficiencies throughout the end-to-end clinical trial process.
Presentation from the 2012 DIA Clinical Data Quality Summit, discussing end-to-end clinical trial automation and CDISC models being adopted from study setup to submission.
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