Empower your Clinical Trial

With increased attention on decentralized trials, a growing number of sponsors and CROs plan to adopt direct data capture (DDC), eCOA, ePRO, and eConsent into their workflows. 

Empower your Clinical Trial​

With increased attention on decentralized trials, a growing number of sponsors and CROs plan to adopt direct data capture (DDC), eCOA, ePRO, and eConsent into their workflows.

The combination of technological advances, proliferation of wearables and regulatory support for DCT adoption demonstrate that remotely-monitored measures and assessments play an integral role in clinical research.

Clinical ink’s platform enables remote participation while providing a single platform that allows patients and sites to switch back and forth among phone, tablet, or web, at virtual or physical sites, as desired. We help you to collect data that matters whether by BYOD, eConsent, telehealth/medicine, and more remote environments.

Centralize Operations and Data

If we are to collect and integrate all this data, especially virtually, data capture practice for clinical trials must be reevaluated. The standard, cumbersome, electronic data capture (EDC) still relies on paper-based source documents, which are then transcribed by site staff into the digital record. Later, this step must be double-checked by monitors (source data verification).

In contrast, eSource direct data capture (DDC) is an efficient alternative better suited to complex workflows and virtual or hybrid situations. It captures data electronically directly into the electronic record at the moment of data creation. Further, a good system integrates all the data sources into a single output that simplifies tracking, evaluation, and reporting for sponsor and CRO teams to recenter decentralized trials.

eSource DDC helps solve the data crisis for virtual and hybrid trials as it:

  • Improves data quality
  • Eliminates duplicate data entry
  • Reduces errors by issuing immediate prompts if data entry is incorrect or incomplete
  • Allows for remote monitoring in real time
  • Enables effective decision-making and issue resolution)
  • Makes data interoperable and accessible
  • Simplifies workflows
  • Cuts costs
  • Reduces timelines

To be competitive in life sciences today, you need to centralize operations and data to power patient science and outcomes.

Benefits for Sponsors

  • Gain immediate access to validated data
  • Accelerate recruitment and improve retention
  • Cut out monitoring charges for lower costs
  • Connect better with productive sites
  • Get automated site analytics and reporting
  • Speed up database lock
  • Enter data ONCE!
  • Use decentralized trial tools to recruit and retain patients
  • Validate data as you capture it
  • Use a single tool for eCOA and other trial data
  • Use a familiar document-based solution
  • Connect with patients easily
  • Do away with source data verification (SDV)
  • Focus on source document review (SDR) – all remotely
  • Focus on the most important data through guided and targeted SDR
  • Record source document audit trail with ease
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