3D Tissue Models
eCTD 2010
Philadelphia City Center

Philadelphia, Pennsylvania


   CHI’s Inaugural eCTD 2010: Achieving Efficiency and Compliance in
   Electronic Submissions will be held March 10, 2010 at the Crowne Plaza
   Philadelphia City Center in Philadelphia, PA. This conference will be
   co-located with the Summit for Clinical Ops Executives ( SCOPE ), a
   four-day cluster of events taking place March 8-11, 2010. eCTD 2010 is
   co-hosted by CHI , Bio-IT World, and eCliniqua and is preceded by its
   partner events, CHI’s Second Annual Electronic Data in Clinical
   Trials, Third Annual Patient Recruitment in Clinical Trials and a
   short course on ’Utilization of Electronic Health Record ( EHR ) Data
   in Clinical Research. Filing new submissions is time consuming and
   costly to both regulators and drug development organizations. Global
   regulatory agencies are committed to improving the approval process
   and the electronic Common Technical Document (eCTD) is seen as a
   practical solution. It has been mandated in some countries and, to
   date, over 30,000 eCTD sequences have been submitted to the FDA alone.
   Despite the promise of eCTD to move your data through the approval
   process more efficiently, there are challenges to adoption and
   implementation. This conference is intended to cover how to achieve
   efficiency and compliance in electronic submissions.

Schedule of Presentations:

Monday, March 8, 2010
Tuesday, March 9, 2010
Wednesday, March 10, 2010
Thursday, March 11, 2010
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