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Delve into a variety of interesting and helpful resources.

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A Symphony of Standards and Partnerships

Posted by Fiona Hartley on Jun 12, 2014 5:19:08 PM

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.

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Topics: CDISC, CROs, Standards, Technology Partnership, Presentations, Study Design

Using CDISC to Optimize New and Legacy Studies

Posted by Fiona Hartley on Apr 25, 2014 4:54:26 PM

Get the presentation from the Formedix learning webinar about optimizing new and legacy studies using CDISC.

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Topics: CDISC, CROs, Legacy Studies, Standards, Data Management, Dataset-XML, Pharma, Presentations

Life is tough as a CRO

Posted by Fiona Hartley on Nov 21, 2013 11:06:01 AM

This infographic illustrates six of the most common challenges that CROs experience in the battle to win sponsor business.

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Topics: CROs, Standards, Infographics, Technology Partnership, Study Build, Study Design, Submissions

CDASH: A Primer and Guide to Implementation

Posted by Fiona Hartley on Nov 19, 2013 10:44:57 AM

Download the slides from Formedix CEO Mark Wheeldon's presentation at the New Jersey CDISC User Group in Merck, Summit, discussing all things CDASH.

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Topics: Biotech, CDASH, CDISC, CROs, Standards, Pharma, Presentations

End-to-End Automation Using CDISC - Formedix and Medidata Partner

Posted by Fiona Hartley on Nov 15, 2013 12:09:40 PM

Hear how Formedix and Medidata have partnered to implement CDISC together across the entire end-to-end clinical trial process, in this webinar recording.

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Topics: Biotech, CDISC, CROs, Standards, Webinars, Technology Partnership, Pharma

Utilizing CDISC to Drive Efficiencies with OpenClinica

Posted by Fiona Hartley on Aug 16, 2013 12:49:47 PM

This presentation discusses real life-experiences of using CDISC Database Standards (Operational Data Model) to drive efficiencies in study setup and study build.

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Topics: Biotech, CDISC, CROs, Technology Partnership, Pharma, Presentations, Study Build, Study Design

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

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

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