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Achieving the 'iTunes' of Clinical Trials

Posted by Fiona Hartley on Aug 16, 2013 11:58:30 AM

This presentation from CDISC Europe Interchange 2013 explains how an ‘iTunes-style’ metadata repository can be established using CDISC standardized content, in a CDISC vendor-neutral model.

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Topics: CDISC, Standards, Presentations, Study Build, Study Design, Submissions

Using CDISC to Optimize End-to-End Trial Process

Posted by Fiona Hartley on Aug 16, 2013 11:55:23 AM

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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Topics: Biotech, CDISC, CROs, Standards, Pharma, Presentations, Study Design

Saving Time and Money in the Clinical Trial Process

Posted by Fiona Hartley on Aug 16, 2013 11:52:07 AM

CEO Mark Wheeldon's presentation from DIA EuroMeeting, March 2012, on how CDISC models can be adopted throughout the end-to-end clinical trial process.

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Topics: Biotech, CDISC, CROs, Standards, Pharma, Presentations, Study Build, Study Design, Submissions

An Efficient and Optimized End-to-End Process Starts with CDISC

Posted by Fiona Hartley on Aug 16, 2013 11:49:19 AM

Formedix CEO Mark Wheeldon presented at ESUG Meeting, November 2012, discussing how the end-to-end clinical trial process can be made more efficient using CDISC standards.

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Topics: CDISC, Standards, Presentations, Study Build, Study Design, Submissions