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.
0 Comments Click here to read/write comments
Topics: CDISC, Standards, Presentations, Study Build, Study Design, Submissions
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.
0 Comments Click here to read/write comments
Topics: Biotech, CDISC, CROs, Standards, Pharma, Presentations, Study Design
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.
0 Comments Click here to read/write comments
Topics: Biotech, CDISC, CROs, Standards, Pharma, Presentations, Study Build, Study Design, Submissions
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.
0 Comments Click here to read/write comments
Topics: CDISC, Standards, Presentations, Study Build, Study Design, Submissions