(Official languages: Spanish and English)

09:30   10:00     Registration & Coffee

10:00 - 10:10    Welcome
                       Cedric Burg, Deputy Head of Global Clinical Operations, TEVA

:10 - 10:50    Study Metrics for Value and Quality - Just Historical Data or Pointers for the Future?
John Shillingford, VP Early Phase Clinical Operations, Aptiv Solutions

10:50 - 11:20    Integration of different data sources in Oracle RDC  read Abstract >>
Valentina Cavestro, Lead Data Manager, CROSnt

11:20 - 11:50    Killing Two Birds with One Stone: Pooling Legacy Data Using CDISC
                       Data Standards  
read Abstract >>
Pantaleo Nacci, Global Head, Statistical Reporting, Novartis Vaccines & Diagnostics

11:50 - 12:10   Coffee Break

12:10 - 12:40    Development of Data Standards and Data Integration tools   read Abstract >>
  Rafael Romero, Director Global Clinical Data Management & eTrials

12:40 - 13:10    Leveraging data from existing information systems for a complete redisign of the
                       standard monitoring visit report used in clinical trials. Impact on the CRA's work and
                       efficiencies created accross the organisation. Overcoming resistance to change for
                       successful implementation  
read Abstract >>
                       Cedric Burg, Deputy Head of Global Clinical Operations, TEVA

13:10 - 13:40    Formación on-line para equipos de investigación a nivel internacional
Marta Manjón, Project Director, Grupo  Rater Training Intenacional, i3 

13:40 - 14:10    Optimise your CTMS according to your Business needs & Information System
read Abstract >>

Diego Herrera, Study Information Manager - Toni Yeste: Clinical Study Information
                       Coordinator, Almirall

14:10 - 15:10    Networking Lunch and Exhibitors Area

15:10 - 15:40    New trends in Clinical development
  Juan Diego Polo Santos, Business Development Director EMEA, Oracle Ibérica
                       Gilbert Bellachen, Director, Global Customer Experience - Oracle Health Sciences
                       Global Business Unit, Oracle France

15:40 - 16:10    Análisis de los factores críticos de éxito (CSF’s) en la implantación de un sistema
                       de recogida de datos electrónico
(SRDE)  read Abstract >>
Luis M. Luengo Pascual, Director General de 3D Health Research
16:10 - 16:30    Coffee Break

16:30 - 17:10    Análisis de riesgos (Risk Management) aplicado a la gestión
                       de datos clínicos 
read Abstract >>

Natalia Arroyo, Biomedical Research Advisor, Telstar Life Science Value Services

17:10 - 17:30    Beneficios y Riesgos del archivo electrónico de un Ensayo Clínico  read Abstract >>
Sonia Marimón, Clinical Trial Assistant, Country Clinical Operations, Pfizer

17:30 - 17:50    Global Survey Results: Analysis of Electronic Data Capture Use in Clinical Trials  
read Abstract >>
Mary Wieder, Marketing Officer, Arithmos

17:50 - 18:15    Networking Cocktail

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