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.
Controlling Timelines and Costs
Maintain and accelerate timelines and milestones, from study start-up to data collection and analysis.
Recruiting and Retaining Patients
Discover patients that meet inclusion criteria, gain consent, and engage to meet adherence.
Ensuring Data Integrity
Ensure data collection, quality, and analysis are accurate and reliable, particularly with complex clinical trials.
Managing Safety and Risk
Minimize the potential for adverse events and ensure each study is conducted ethically.
Meeting Regulatory Requirements
Comply with a wide range of regulations governing trial conduct to ensure compliance and avoid setbacks.
Powering Collaboration
Enable study teams, investigators, CROs, and other stakeholders with tools to ensure trial efficiency.
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-centric research.
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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