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Non-CDISC Events

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  • 28 January: Database Updates
  • 25 February: Lab Data
  • 18 March: CDISC
  • 22 April: Data Management Plans
  • 20 May: Managing Virtual Teams
  • 17 June: Overall Clinical Trials Process, Roles and Responsibilities
  • 16 September: Touch Point/Hand Offs (with SAE Reconciliation)
  • 18 November: Protocol Review

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Call for Posters for DIA/FDA Computational Science Annual Meeting
Bethesda North Marriott, Bethesda, MD

Suggested Poster Abstract Topics – Poster submissions due March 1, 2010

  • Data submission standards development, implementation, and best practices
  • User experience/evaluation of current processes and tools and the subsequent impact on organizational performance
  • Needs and specifications for proposed new tools and processes
  • Business processes driving information systems development
  • Impact of processes and tools on problem solving quality, efficiency, and cost

Submit a Poster Abstract


Key CDISC Presentations

Monday 22 March 2010

13:00 - 14:30 Plennary Session 3, Data Standards: Working on the Vision and Taking the Next Steps

Dr. Rebecca Kush presents:

Planning the Clinical Research Process with Your Submission in Mind


Tuesday 23 March 2010

10:15 - 12:15 Session 6: Breaout Sessions, Data Quality

Dave Iberson-Hurst presents:  

Use of Electronic Health Records and Electronic Data Capture for Real Time Monitoring

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e-Clinical Trials Conference

 

 

 

18-19 May 2010, Munich, Germany

 

The 10th annual e-Clinical Trials Conference will bring together pharmaceutical companies to share their experiences and to present practical examples of end to end, fully integrated e-clinical trials processes.


It is the wide mix of attendees at conference that makes this the primary event on the topic of how the whole e-clinical mix is improving the various functional areas of clinical trials and ways you can maximise your costs and time savings.


As a result of detailed research with experienced professionals involved in clinical trials throughout Europe, a wide range of critical topics will be debated at this exciting event, including:

  • How to manage the evolving e-clinical trials landscape and technology
  • Fast and efficient implementation of EDC
  • A practical approach to the new technology and how this has affected monitoring trials

plus much more.


Register your place NOW by CLICKING HERE and receive 10% off the conference fee - this event WILL sell out! 

For more information email: emahnhauari@arena-international.com, or call +44 207 936 6672.

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New CDISC Member Application

To register for a new membership, please supply the following information.

MEMBERSHIP OF CDISC IS NOT FREE AND IS FOR COMPANY MEMBERSHIP NOT INDIVIDUALS.

Please read the details on the membership page BEFORE you apply.

Please also check that your company is not already a member of CDISC here: CDISC Members.






If you selected Corporate Benefactor or Sponsor, enter the name and email address of CDISC Advisory Board (CAB) member.
















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