CHI`s Annual `Electronic Data in Clinical Trials` (at SCOPE) 2017 is one of the conferences within the SCOPE Summit.
CHI`s Annual `Electronic Data in Clinical Trials` (at SCOPE) 2017 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)
CHI`s Annual `Electronic Data in Clinical Trials` (at SCOPE) 2017 brings together clinical operations executives.