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CRF Health has used its thorough understanding of drug development and mobile technology to create TrialMax®. The suite is the first electronic diary tool to design, manage and host global ePRO Phase I to IV studies capturing data via PDA devices.
In the past, electronic diary design required manual programming of each study into the PDA device. This was time consuming, inflexible and often error prone. This old design methodology offered no way to collaborate with the client study teams, which is necessary for a clinical trial to be successful.
The TrialMax® suite’s eDiary design tool, TrialStudio™ is the only ePRO software solution on the market that offers a truly collaborative approach to the eDiary design process. The design tool’s real-time development capabilities allow CRF Health, together with the client study team, to design and adapt the trial questionnaire instantly saving both time and money.
Already used across 61 countries and in 68 languages for 45 indications, our eDiary solutions are scalable and can deliver studies with tens of thousands of patients across hundreds of sites, and has user acceptance from children to the elderly and terminally ill.
TrialMax® provides the following tools:
- TrialStudio for designing eDiaries in collaboration with the client study team
- TrialCollector for fast and reliable data capture from patients; and
- TrialManager, an online web portal for comprehensive patient and compliance management
By using TrialMax® sites and study teams can:
- Manage patients proactively by viewing patient reported data and study-specific reports of patient data, such as real time compliance information and eligibility assessments.
- Manage use of study medication by monitoring compliance to medication schedule, dosage titration, recording concomitant medication, monitoring effects and efficacy and proactive clinical decision making on an individual patient basis.
- Capture high-quality data with an average 90% compliance rate by using alarms, patient reminders, intelligent branching logic, and edit checks. All data is attributable and verifiable with date and time stamp and full compliance with 21 CFR Part 11.
- Manage the study by using real time study data and customized reports that meet each study's needs as well as online download of study data, matched to each study's own standards and formats.
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