Non-CDISC Events

• 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

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

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.