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Resources

Catch up with the thought leaders at Clinical Ink, learn more about our specific clinical trial technology solutions and support and stay up-to-date with the latest news in the industry.

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Tips For Reducing Site Burden - And the Benefits of eSource and eCOA

Innovation in ePRO for Questionnaire Data Capture

eSource Survey Results - How Sites can Benefit from Paperless Clinical Trials

ePRO Translations Re-Imagined: Opening Another Black Box of ePRO

BYOD for ePRO Study Results: Addressing Risks and Leveraging Benefits

Configuration in ePRO

Implementing BYOD Across Phase II and III Clinical Trials

Speeding R&D Via Video and Imaging Powered by Remote Monitoring

Accelerating Database Lock via Adaptive Design, Remote Monitoring

Guiding Protocol for Research Naïve Sites to Expand Patient Access

Enabling Offline, Remote Clinical Research & Ensuring Data Security

Delivering Data in Minutes with Remote Monitoring to Reduce R&D Timelines, Costs

Supporting Multiple Simultaneous Studies to Reduce Timelines, Streamline Development

Capture 6: Improve Protocol Execution by Reducing Errors and Site Burden

eCOA/ePRO Patient Engagement

eCOA/ePRO For all of your eCOA and ePRO needs at home and on-site

Capture: Reducing Site Workload for Better, Faster, Safer Clinical Trials

Phase 1 Clinical Trials and ePRO: The Time is Now

The Impact of mHealth on Protocol Compliance and Subject Dropouts in Clinical Trials

Putting Patients and Sites at the Center of Your Clinical Trial

ePRO and Agile Methodology: A Winning End-to-End Solution for Oncology Studies

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