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Track 55: E-Clinical Technologies

Track 55: E-Clinical Technologies

Overview: eClinical Technologies

eClinical Technologies refer to a suite of digital tools, platforms, and software systems used to plan, manage, and conduct clinical trials more efficiently and accurately. These technologies streamline data collection, trial management, monitoring, and reporting processes, reducing manual errors and improving regulatory compliance. Adoption of eClinical solutions has rapidly increased due to the complexity of modern trials, the rise of decentralized trials, and the need for real-time data access. These technologies improve patient engagement, site performance, and trial transparency while lowering overall costs.

Key Sub-Topics in eClinical Technologies:

Electronic Data Capture (EDC) · Clinical Trial Management Systems (CTMS) · Interactive Response Technology (IRT/IWRS/IVRS) · Electronic Patient-Reported Outcomes (ePRO/eCOA) · Remote Source Data Verification (rSDV) · Electronic Informed Consent (eConsent) · Risk-Based Monitoring Tools · eTMF (Electronic Trial Master File) · Wearables and Mobile Health Apps · Real-Time Data Analytics Dashboards · Site Performance and Risk Tracking · Cloud-Based Trial Platforms · Decentralized Clinical Trial Tools · Integration with EMR/EHR Systems · Regulatory Compliance (21 CFR Part 11, GDPR)