Sponsors

Achieve Clinical Trial Success​

Achieving clinical trial success is increasingly challenging for Sponsors. 

Complex study designs, exponential data volumes from disparate sources, and competition for sites, as well as patient safety and satisfaction are a few among many obstacles.

By adopting Clinical ink eSource technology and tools, Sponsors can manage patient recruitment, adherence, study site relationships, data privacy, and regulatory requirements with speed, transparency, and quality.

Why Clinical ink for Sponsors

Clinical ink enables Sponsors with its eSource technology and suite of built-for-purpose tools. By collecting and managing clinical trial data electronically, rather than using paper forms, Sponsors gain real-time data entry, validation, and cleaning.

eSource Solutions for Sponsors

Integrating Direct Data Capture (DDC) technology, eCOA, ePRO, and eConsent into workflows enables Sponsors to improve the capture, visibility, and management of data across devices, sensors, telemedicine, and digital health technologies (DHTs).

Capture What’s Needed, Anywhere

Collect all data, regardless of whether its novel, simple, or complex.

Improve Site and Patient Readiness

Discover, train, and educate all stakeholders.

Execute Rapidly and Flexibly

Expedite builds and confidently configure diverse model.

Eliminate Gaps in Collaboration

Share protocols, documents, and data instantly.

Improve Patient Engagement

Simplify recruitment and data gathering with an all-in-one clinical trial software technology.

Enhance Data Quantity and Quality

Direct data capture boosts the amount and quality of your trial data.

Recenter Decentralized Trials

Centralize data and operations to power patient science.

Manage Global Logistics

Gain control of deployment and monitoring of devices and technologies.

How a Remote ePRO Solution Helped Reduce Patient Burden

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eSource: Your Path to Clinical Research Optimization

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