[IEEE-bhpjobs] Fwd: Free Webcast Jun 8 on Why Clinical Development Teams Should Care about Data Standards Part III and Upcoming Clinical Management Congress

Tue May 23 12:12:18 EDT 2006

-----Original Message-----
From: Sheila Camhi [mailto:news at cdisc.org]
Sent: Tuesday, May 23, 2006 07:15 AM
To: esther-l at mailsnare.net
Subject: Free Webcast on Why Clinical Development Teams Should Care about Data Standards Part III and Upcoming Clinical Management Congress

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Why Clinical Development Teams Should Care about Data Standards- Part III: Real World Experiences with the ODM (audio seminar)
Free Webcast Sponsored by BetterManagement.com, AMIA and CDISC

Date: 8 June 2006, Thursday

Time: 8:30 AM- 9:30 AM Los Angeles Daylight 
Time

10:30 AM- 11:30 AM Chicago Daylight Time

11:30 AM- 12:30 PM New York Daylight Time

Register Now (http://rs6.net/tn.jsp?t=jd4wtvbab.0.ib5pxvbab.btzkurbab.893&p=http%3A%2F%2Fwww.bettermanagement.com%2Fseminars%2Fseminar.aspx%3Fl%3D13792)

This Webcast 
is part of the 2006 Global Strategies for Clinical 
Trial Information (http://rs6.net/tn.jsp?t=jd4wtvbab.0.pb5pxvbab.btzkurbab.893&p=http%3A%2F%2Fwww.bettermanagement.com%2Fseminars%2Fdetails.aspx%3Fl%3D13852) series sponsored by CDISC  (http://rs6.net/tn.jsp?t=jd4wtvbab.0.45p7atbab.btzkurbab.893&p=http%3A%2F%2Fwww.cdisc.org%2F)
and AMIA (http://rs6.net/tn.jsp?t=jd4wtvbab.0.tb5pxvbab.btzkurbab.893&p=http%3A%2F%2Fwww.amia.org%2F).

Presentors Ed Helton, SAS and Gary Walker, 
Quintiles will facilitate a 45 minute presentation and a 
15 minute Q & A. 

Program content

In the previous webcasts on the ODM, attendees 
have learned about the ODM, its role and the means 
by which it has been extended to support the 
submission of clinical trial data to the FDA.  In this 
webcast, attendees will hear from those who have 
used the model in the submission process, as well as 
from the agency who will receive these submissions 
for the review and approval process.

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
Clinical Trial Management Congress

In association with CDISC, Oxford International is 
pleased to announce the Clinical Trial
Management Congress, to be held in Park Hyatt Hotel 
in Bellevue, Philadelphia, USA on 6th-7th 

November 2006.

In keeping with Oxford International's highly 
successful
 pharmaceutical technology series, an 
exemplary panel of industry speakers, including 
representatives from Serono,

Pfizer, Boehringer-Ingelheim, AstraZeneca and many 
more 
will be present to share up-to-date 
information on industry topics.The programme will 
address key industry topics

including eClinical trial technologies, clinical trial 
management strategy, patient recruitment and 
outsourcing, parternship and alliance mangement.

The congress presents an ideal opportunity for you  
to raise your profile, become fully up-to-date on the 
most recent developments in the industry, meet 
peers, catch up on latest research and gain
information on new services.

To recognize CDISC's partnership with this 
event, Oxford International is able to offer a 10% 
discount on delegate registration to members quoting 
the reference CTMCDISC.
  For more information 
on delegate registration please visit the event 
website or contact Joanne Taylor on +44 (0) 870 890 
3303 or by emailing: joanne.taylor at oxfordint.co.uk

DATE: 6th-7th November 2006
LOCATION: Park Hyatt Hotel, Bellevue, Philadelphia

For more information on delegate registration please click here - http://rs6.net/tn.jsp?t=jd4wtvbab.0.vb5pxvbab.btzkurbab.893&p=http%3A%2F%2Fwww.clinicalcongress.com

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
Learning Objectives
------------------------------------------------------------
Why Clinical Development Teams Should Care about Data Standards: Part III

In this session attendees will learn:

About the real-life experiences of using the ODM 
to support the submission of clinical trial data.

Why this is important to pharmaceutical 
companies.

Why this is wanted by the agency.

---

Clinical Trial Management Congress

The congress offers attendees an uprecedented 
opportunity to network with leading senior-level 
clinical trials and technology executives,to identify 
successful strategies in maximizing clinical trial 
productivity, through the applicationof e-clinical 
technologies, and effective patient recruitment and 
outsourcing strategies.

---

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
CDISC Staff
Clinical Data Interchange Standards Consortium
------------------------------------------------------------

email: news at cdisc.org
phone: 512-341-9885
web: http://www.cdisc.org

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