CHI`s Annual `Electronic Data in Clinical Trials` (at SCOPE) 2012

February 7 - 9, 2012(Ended)

Hilton Miami Downtown Hotel
Miami, FL, United States

Electronic Data in Clinical Trials is one of the conferences within the SCOPE Summit.

Electronic Data in Clinical Trials covers topics such as:

Approaching data integration for BioTech and Pharma: Integrating systems (IVRS, EDC and CTMS) and clinical operations data
Utilization of Electronic Health Record (EHR) data in clinical research: Overcoming policy, regulatory, organizational and technical challenges
Incorporating and integrating the eClinical systems and practices of two organizations: Lessons learned in the latest set of mergers
Increasing clinical trial efficiency through operational data management: Best practices in integrating safety reporting data and your EDC system
Available technologies and vendor selection
Electronic Data Capture (EDC) adoption: Changes in processes and procedures and training staff (site, sponsor staff and CROs)
Enable the patient-centered clinical trial by integration of mobile and web-based technologies
Regulatory compliance issues on the use of computerized systems in clinical investigations: Regulatory audits at sites using EDC and Qualification of sites that have EMR/HER systems for source documents
E-Diaries: Ease of use and compliance in various populations and consistency of data with data previously collected by paper diaries
Enable adaptive trials by leveraging technology
Practical implementation of CDASH recommendations
Information security and EDC: Safeguarding the security and reliability of Electronic Clinical Trials (ECT)