The Program Committee is currently accepting abstracts for presentations and posters at the 2017 CDISC Europe Interchange in London, UK 24-28 April 2017. Click below to submit your abstract by 13 January 2017 Central Europe Time.
Increase the visibility of your organization by sponsoring a CDISC Interchange. View sponsorship details to learn about the various opportunties available to your organization.
Description:This year's IntraChange will follow the same general pattern as the 2014 Winter IntraChange, consisting of individual team and cross-team meetings devoted to accomplishing 2015 CDISC team goals and to address key topics of interest to CDISC teams. The meeting will also include opening plenary sessions each day including informative training sessions on plans, use of Jira and Wiki collaboration tools, using SHARE for standards development, and optimizing the standards development process. Team meetings will include ADaM, CDASH, COA/QS, SDS and XML Technologies.
Hyatt Regency Chicago Reservation Secure your hotel reservation by 21 October (or until rooms are no longer available) at the discounted attendee rate of US$249. The Hyatt Regency is located next to the Fairmont Chicago where the International Interchange will take place.
Join us and hear from EMA, FDA, and PMDA who will be speaking at this event. View our distinguished speakers here.
A special FDA Reviewer session is offered at this event.Click here for description.Deadline for offline registration for the FDA Reviewer Workshop is Wednesday, 29 April. After 29 April, offline and onsite registrations cannot be accepted for this session.
Registration for the CDISC Symposium on 16 May 2014 is open now, click here.
To register for CDISC Education Courses on 19-21 May 2014, click here.
$50 for CDISC Platinum Member (Gov't/Academic/NonProfit)
$60 for Gold Member
$70 for Non-Member
13:30-14:00 PMDA’s presentation
14:00–15:30 A Global Approach to Accelerating Medical Research (1st half)
15:45–17:15 A Global Approach to Accelerating Medical Research (2nd half)
What is the CDISC Symposium?
The CDISC Symposium in Tokyo, Japan is a half-day seminar that will include essential information on the significant benefits of using CDISC standards from the start of clinical research studies through study conduct, analysis and reporting. Presentations will be given by Dr. Rebecca Kush, CDISC President and CEO; Shannon Labout, CCDM, CDISC VP of Education; and Yuki Ando of the PMDA. The topics covered will include “What is CDISC?” and “Why CDISC Now?” A presentation on PMDA’s plan for utilizing CDISC standards will also be given.
Who Should Attend the CDISC Symposium?
We anticipate that the audience that attends the CDISC Symposium will not only be programmers and data managers, but also various types of pharmaceutical representatives including, but not limited to: senior managers, project managers, regulatory personnel, clinicians, statisticians and CRAs.
CDISC Education Courses also Available!
This event is part of several days of workshops and educational courses that will be offered in Tokyo on 16, 19-21 May 2014. The CDISC Symposium will be held on 16 May, and the following week CDISC Educational Courses will be held on 19-21 May. Interested individuals can register for one or both of these events based upon their interest. To register for the CDISC Education Courses that will be held on 19-21 May, please click here .