Great design is essential to a successful clinical trial: intuitive, user-friendly eCOA solutions drive high compliance rates and clean, accurate data. That’s why CRF Health’s design process, powered by TrialStudio™, is collaborative, interactive and agile.
Instead of waiting weeks, your team receives a working prototype as early as our first meeting. We create your eCOA questionnaires quickly, make changes with ease and provide peace of mind through transparency into the entire process.
Securing informed consent from clinical trial participants involves more than a signature—you
to ensure they truly understand what they’re signing.
A critical first step, consent has a major impact on regulatory compliance, enrollment rates and expenses across the life of your study.
Intuitive and interactive, TrialConsent™ promotes participant compliance and retention through better comprehension. The only solution offering eConsent and eCOA on a single integrated device, TrialConsent™ can be conveniently deployed via TrialMax Slate® or as a standalone web-based solution.
Comprehensive reporting enables study teams and ethics committees to monitor the consent status of sites and participants, track and analyze compliance and make smarter decisions.
Electronic Clinical Outcome Assessments (eCOA) fit seamlessly into subjects’ real lives, guiding them through the study protocol, driving high compliance, and generating clean data. CRF Health’s integrated TrialMax® software platform is the ultimate eCOA solution for clinical trials from Phase I to Phase IV and beyond, with four modalities to suit your study’s particular needs.
Put eCOA technology directly in your patients’ hands, anytime and anywhere. Mobile, intuitive and easy-to-use, TrialMax Touch fits into subjects’ real lives to fuel high compliance and complete data. With expertly designed eCOA instruments on provisioned handheld devices, TrialMax Touch is an ideal solution for Phase II and Phase III trials.
Make data collection easier than ever for your site team and patients with TrialMax Slate. CRF Health’s dedicated tablet solution for collecting site-based PROs, ClinROs, ObsROs and PerfROs expedites enrollment, entry and management.
Simplify and streamline late-phase studies to establish your product’s value and long-term safety with TrialMax Web. CRF Health’s web-based mobile-friendly eCOA solution is ideally suited for large Phase IV trials, especially those with infrequent data collection schedules.
Empower patients to submit eCOA data on their own mobile device with TrialMax App. CRF Health’s collaborative design process in TrialStudio™ enables us to customize the TrialMax App for your study’s needs quickly and easily.
Monitor and manage your eCOA clinical trial data in real-time with TrialManager™. CRF Health’s online portal makes it easy to instantly explore and review data collected from any TrialMax modality. Discover meaningful insights and drive smarter decisions with next-generation data visualization reporting tools.