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Define 2.0 - What's New?

Posted by Fiona Hartley on Aug 16, 2013 12:47:34 PM

This white paper shows, at-a-glance, the new features and improvements in the latest version of this CDISC standard and its day-to-day use.

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Topics: CDISC, Define-XML, Study Build, Study Design, Submissions, White Papers

Discover Define-XML: Practical Uses End-to-end Today

Posted by Fiona Hartley on Aug 16, 2013 12:37:41 PM

Formedix CEO Mark Wheeldon's presentation from the 2013 Bay Area User Group, which looks at practical uses of Define-XML in the end-to-end clinical trial process.

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Topics: CDISC, Define-XML, Presentations, Study Build, Study Design, Submissions

Define-XML Tools - David Borbas

Posted by Fiona Hartley on Aug 16, 2013 12:34:46 PM

Presentation by David Borbas, Jazz Pharmaceuticals discussing Define-XML at our executive breakfast as sponsors of the Bay Area User Group.

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Topics: CDISC, Define-XML, Presentations

CDISC Strategy 2013-2015  - Rebecca Kush

Posted by Fiona Hartley on Aug 16, 2013 12:32:36 PM

CDISC President Rebecca Kush presented at our executive breakfast prior to the Bay Area User Group, discussing CDISC's strategy from 2013 - 2015.

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Topics: CDISC, Standards, Presentations

End-to-End Standards Enable Clinical Trial Efficiencies

Posted by Fiona Hartley on Aug 16, 2013 12:29:51 PM

Presentation from Formedix-hosted Bay Area Executive Breakfast, discussing standards to enable efficiencies throughout the end-to-end clinical trial process.

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

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

FDA Study Data Exchange Standards

Posted by Fiona Hartley on Aug 16, 2013 11:45:11 AM

This Technical Expert opinion piece explains why CDISC is our chosen solution for a Study Data Exchange Standard, time and time again.

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Topics: Biotech, CDISC, CROs, Standards, Pharma, White Papers