CliniTrial is a mobile, cloud-based eSource solution, transforming the clinical trial industry. It is designed using cutting edge technology leveraging SMAC (Social, Mobile, Analytics & Cloud). It helps eliminate several inefficiencies and manual processes, and streamlines the data collection, data analytics and data submission workflow. Sponsors also get instant visibility of study KPI’s, with real-time reporting/analytics and several rich capabilities.
We give you unprecedented speed and agility
Our intuitive point & click interface with extensive built-in CDASH form libraries, variables, dynamic form rules and custom skip logic will not only help in having consistent configuration across multiple studies but will also help in post-study data management. The study setup is usually a matter of days/weeks than months.
Rely on our reporting system
Improved decision making with near-real time updates from across sites. Our rich reporting capabilities will empower you to prepare reports, analyze trends, find discrepancies, monitor site compliance, and identify underperforming sites to ensure that your trials stay on track.
We offer flexibility and streamlined workflow
Seamlessly introduce mid-study changes without spending weeks on database lock, data migration and site coordination. Leverage CliniTrial to update the study requirements via the portal and send your updated study configuration with push notification on mobile devices.
Collect your data offline
Capture data offline using tablets and synchronize the data online. CliniTrial makes data collection using mobile devices easy, quick, and accurate with a user friendly interface, instant edit checks, lab data import, photo/video upload capabilities etc. With CliniTrial, you are fully functional without the dependency on internet connection.
Integration is the solution
Reduce your data collection time and increase your data quality by utilizing our integration features. CliniTrial integrates with various medical devices and software to automate and streamline the data collection procedure and significantly cut down on verification costs.
Leverage CDISC compliant solution
Use eCRFs from our CDASH compliant library to generate CDISC-compliant SDTM datasets. Your eCRF design time will be shortened as CDASH eCRF forms can be pulled out of our library. FDA recommends CDISC data standards, and will in the near future require all submissions to be CDISC-compliant.
We have the solution
CliniTrial is validated and compliant with 21 CFR Part 11 and HIPAA. It is designed with a high focus on data integrity, data security and data compliance, with features including audit trails, time stamps, date stamps, encryption and remote data control via mobile device management (MDM) solution.
Use our site analytics
With our site level dashboard get a quick overview of your site performance and also compare your site metrics with other sites, in the study. All our metrics are based on SMART attributes (Simple, Measurable, Actionable, Real, Timely) so sites can focus on KPI that matter.
CliniTrial gives you all the benefits
Our tablet based eSource solution, can be seamlessly integrated with other eClinical tools to offer you the benefits of offline data capture, medical device integration, multi-lingual support and various other benefits and enable you to streamline your data sourcing, data management, reporting requirements.