Electronic Data in Clinical Trials 2012

Cambridge Healthech Institute (CHI) is pleased to announce the production of Electronic Data in Clinical Trials: Collecting and Leveraging Data to Optimize Clinical Trials being held February 7-8, 2012 at the Hilton Miami Downtown in Miami, FL.

The gathering will once again be co-located within the Summit for Clinical Trials Operations Executives (SCOPE), a three-day cluster of events that attracted 400 leaders in clinical operations and research in February 2011. CHI’s Fourth Annual Electronic Data in Clinical Trials will be preceded by a short course on EMR/EHRs: Utilization of Electronic Health Record (EHR) Data for Registration Studies and then followed by a new sister event, Integrating and Leveraging Clinical Trial Operations Data: Portals, Data Warehouses, Site/Study Execution Metrics. Please see the program map below for 2012. Topics to be discussed include:

-Utilization of Electronic Health Record (EHR) data in clinical research: Overcoming regulatory, policy, technical and organizational challenges

-Approaching data integration for BioTech, Small/Midsize Pharma and Big Pharma: Integrating systems (EDC, IVRS, CTMS) and clinical operations data

-Increasing clinical trial efficiency through operational data management: Best practices in integrating safety reporting data and your EDC system

-Incorporating and integrating the eClinical systems and practices of two organizations: Lessons learned in the latest set of mergers

-Electronic Data Capture (EDC) adoption: Changes in processes and procedures and training staff (sponsor staff, site, CROs)

-Available technologies and vendor selection: Selecting the right partner for your strategy

-Regulatory compliance issues on the use of computerized systems in clinical investigations: Qualification of sites that have EMR/EHR systems for source documents; Regulatory audits at sites using EDC

-Integration of mobile and web-based technologies to ena