We know that investigative site staff need to be as productive and effective as possible to ensure their clinical trial is a success. Electronic patient diaries have revolutionized the way study teams manage the clinical trial process – reducing costs, time and effort and increasing patient compliance and data quality. The benefits we provide to sites include:
Real Time Diary Design: CRF Health is the only ePRO provider that offers a truly collaborative approach to the eDiary design process. Our design tool’s real-time development capabilities allow us to work together with the site manager to design and adapt the trial questionnaire instantly, typically giving the trial team an extra five weeks study set-up time.
Data Management: CRF Health improves compliance rates using features such as alarms, reminders, intelligent branching logic and edit checks. The average eDiary compliance rate is 90%.
Reports Management: CRF Health provides real-time data, allowing site staff to follow up immediately on any noncompliant behavior. We also provide data formats matched to each trial’s own standards with customized reports that meet each site's needs.
|
