"With paper, there is a much higher workload going through every daily diary entry with a patient and having to record that information. With the LogPad, it's all automatic, and doesn't take away from the data management person's time."

Nadia N. Hansel
MD, MPH Instructor, Division of Pulmonary and Critical Care Medicine
Johns Hopkins University
Asthmatx AIR2 Trial

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NEVER USE PAPER AGAIN.

What is ePRO?

Electronic medical diary: the only reliable method to collect subject self-reports and manage the data in real time, medical electronic tool for capturing clinical trial research data.

Benefits of ePRO

How ePRO improves clinical trial data quality and trial management

FDA Guidance on PRO

FDA Guidance supports the use of ePRO in clinical trial research

Return on Investment

Reduced data variance, smaller trials, improved safety and faster decisions

Regulatory Considerations

PHT ePRO system compliance with regulatory requirements

The Future of ePRO

Adaptive sample sizing, email alerts, ePRO-enabled cell phones, cognitive assessments and medication compliance

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