WHITE PAPER
Reduce trial complexity, improve data quality and support patient-centric trial conduct with automated, real-time data capture.
Powering eSource Clinical Trials and Electronic Data Capture
The rise of remote patient trial participation is driving a greater need to adopt eSource technology. eSource enables sites, sponsors, and CROs to adapt and propel their clinical data capture technology, while meeting new expectations for patient centricity.
Leading the way to re-center Decentralized Clinical Trials (DCTs) by connecting data and operations, Clinical ink is the only company to deliver eSource solutions into a single clinical data platform supporting end-to-end clinical development.
eSource Technology and Solutions
Integrating Direct Data Capture (DDC) technology, eCOA, ePRO, and eConsent into workflows improves the capture, visibility, and management of data across devices, sensors, Televisit, and digital health technologies. This proven approach eliminates any need for heritage EDC systems fraught with delays and data inaccuracies due to paper, transcriptions errors, and SDV.
Discover the eSource Model
Select any area of the eSource diagram below to see quick highlights about each solution.
Select “Add to Cart” as you go. At the end of your exploration, click “Get Resources” and enter your contact info. Your eSource library will be forwarded to you.
Unified Data
Platform
Discover the eSource Model
Select any area of the eSource diagram to see quick highlights about each solution.
Select “Add to Cart” as you go. At the end of your exploration, click “Get Resources” and enter your contact info.
Your eSource library will be forwarded to you.
Direct Data Capture
Fact Sheet
eConsent
Fact Sheet
Televisit
Blog Post
eCOA
Fact Sheet
Mobile Device & Tech
Blog Post
Sensors & Wearables
Fact Sheet
Digital Biomarkers
White Paper
Adherence
Fact Sheet
Indirect Data Capture
Fact Sheet
ECGs
Fact Sheet
Imaging
Fact Sheet
Labs
Fact Sheet
Optimize Data Capture with eSource
Clinical development, operations, and IT leaders seek to rationalize and optimize the mix of technology and virtual clinical trial platforms offered by software providers.
Clinical ink enables the collection, aggregation, integration, and classification of clinical data into the eSource ecosystem.
Manage complex data capture in optimal, scalable, sustainable, and customizable ways–all by ensuring real-time collection of quality data at the source with the best clinical data capture technology. Accelerate data analysis for insight-based decisions based on situational awareness by all stakeholders.
DDC Benefits
Gain real-time data collection to drive faster insight-based decisions and better patient outcomes.
- Greater patient engagement and retention
- Faster anomaly detection
- Leaner query resolution
- PV safety surveillance
- Simpler site performance
Enabling Sponsors
DDC delivers on-time and on-budget study management and ensure:
- Accelerate decisions with real-time insights
- Improve oversight and patient safety
- Manage clinical trial functions in-house for greater data control
- Develop therapeutic-area-specific instruments according to best practices
- Achieve and maintain cost savings
Powering CROs
Create new revenue streams by initiating DDC and powering Sponsors with eSource technology.
- Integrate eConsent, ePRO, and/or eCOA in a single ecosystem
- Offer expanded decentralized trial capabilities
- Improve risk management and compliance with greater control
- Maximize internal resources, capabilities, and allocation
