Webinar 1
Date: Thursday, July 30, 2009
Time:
Chicago 07:30 - 09:00 CDT
New York 08:30 - 10:00 EDT
Los Angeles 05:30 - 07:00 PDT
Central European Time 14:30 - 16:00
UK 13:30 - 15:00
To register for Webinar 1
Click here for on-line registration (credit cards only)
Click here for off-line registration (non-credit card payments)
Description
Webinar One will cover the CDASH basics; assumptions, designations, controlled terminology and how use of the CDASH standard will optimize data collection from both the Site and Sponsor perspectives.
Learning Objectives
At the conclusion Webinar 1, participants should be able to:
- Describe the benefits of CRF standardization for investigative sites and other stakeholders in clinical research.
- Explain how CDASH collection fields can be used to create basic CRFs and XML style sheets and how this will facilitate good CRF design and minimize collection of unnecessary data elements and ensure consistency across a clinical program.
- Describe how CDASH data collection fields are related to other CDISC standards, specifically the SDTM and CDISC Controlled Terminology.
Speakers
Melissa Binz, Director, Central Standards Group, Wyeth
Rhonda Facile, Director, CDASH Project, CDISC
Shannon Labout, Principal Consultant
Speaker Bios