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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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Managing Complex Cognitive Batteries and Rater Assessments to Ease Site Burden

How to Minimize Time and Cost of ePRO Translation

Operation Collaboration

Make Data Central to Your CNS Pain Trials with Data Capture Solutions

eConsent Saves Time and Increases Patient Engagement in Clinical Trial Startup

The Lumenis™ eSource Direct Data Capture Solution

How Direct Data Capture is Key for Virtual Clinical Trials’ Comeback

eCOA Solutions Capture and Validate Data Faster and Better, in Real Time

Translation Transformation: How to Minimize Time and Cost of ePRO Translation

Deploy Configurable, Fit-for-Purpose ePRO Solutions, Fast

COVID-19 & The Virtual Trial Rush: Front-Line Insights

Managing Clinical Trial Data Collection for Success During and After COVID-19: From Virtual Trials, EDC to DDC, BYOD, and Beyond

Clinical Data Certainty From Source To Submission: Addressing Data Challenges With eSource

Virtual Trial Solutions for CROs

Managing Trial Data Collection for Success

Improve GI Data and Patient Engagement With GI ePRO/eCOA

Trial Site News Podcast: Hybrid Clinical Trials During and Post-COVID-19

The Electronic Lupus Assessment Suite (eLAS™) for SLE Clinical Trials: A Disease-Specific eCOA/ePRO Application

EDC Versus DDC: Why It Matters

The Future Impact COVID-19 Might Have On Clinical Trial Design

Virtual Trials: Trust in Experience, Trust in Lumenis™

The Future Is Now: EMA Qualification Favors Clinical Trial eSource Solutions Over Outdated Processes

eLAS (Electronic Lupus Assessment Suite) for SLE Clinical Trials

How Smart Technology Is Influencing and Ultimately Improving Clinical Research

Look behind the lecture: real-world evidence in regulatory decision making

Approach Your Risk-Based Monitoring Strategy With Confidence

Embracing Risk-Based Monitoring: The Pivotal Role of Tools and Technologies

Rerouting Your Risk-Based Monitoring Strategy: Overcoming implementation roadblocks with new technologies and approaches

Overcoming the Industry’s Data Crisis

A CRO’s Road to ePRO Revenue

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

Successful BYOD in Any Phase

Clinical Ink and CRO Partner to Create a Disease-Specific Solution to Facilitate Lupus Clinical Trials

Solutions for Complex Trials: How ePRO Can Improve Gastrointestinal Trial Success

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

Putting Patients and Sites at the Center of Your Clinical Trial

Implementing BYOD Across Phase II and III Clinical Trials

How to Leverage eCOA for Improved Signal Detection in Pediatric & Rare Disease Trials

Configuration in ePRO: Making Design More Collaborative & Delivering Better Results

BYOD for ePRO Study Results: Addressing Risks and Leveraging Benefits

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

Speeding R&D: Video & 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: Remote Monitoring Reduces R&D Timeline & Costs

Supporting Multiple Simultaneous Studies to Reduce Timelines, Streamline Development

Improve Protocol Execution by Reducing Errors and Site Burden

eCOA/ePRO Patient Engagement

eCOA / ePRO: For All of Your eCOA & ePRO Needs at Home & On-Site

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

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

Innovation in ePRO for Questionnaire Data Capture

Tips for Reducing Site Burden & the Benefits of eSource & eCOA

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