TrialMaster®
The Most Intuitive EDC Suite on the Market
Featuring superior usability and flexibility, TrialMaster® is the EDC solution for Phase I – IV clinical trials
With early phase clinical trials, we need to enter data in real time, which means the quality of data must be checked as it is being entered. Edit checks must be approached by defining unique metadata for each item such as time tolerances for procedures, soft and hard parameter ranges for numerical fields and calculations occurring in real time as data is entered. The ability to create custom validation checks, such as ensuring one date is after another date is also supported. To round off the data management features, queries can be routed, data reviewed and the study-locked-data exported in recognizable formats such as SAS Transport files.
TrialOne is a comprehensive set of modules that drive efficiencies, reduce timelines and reduce costs through faster and more directed volunteer recruitment; easy-to-build, schedule-based workflows; real-time, bedside data collection; direct data capture from devices; sample-processing automation and modern data processing. The browser-based, tablet-compatible system provides an advanced platform for automating your clinical operations, complies with FDA 21 CFR Part 11 and supports CDASH data standards for faster and easier exporting and reporting of data. TrialOne is designed and developed by early phase experts to deliver early phase trials in a way that is adaptable to the way you work.
Early stage researchers, including Phase I Clinics and Units, with limited resources now have access to T1xpress, a new eClinical research option designed to accelerate and enhance clinical operations.
With preset configurations, T1xpress enables researchers with limited resources to automate their facilities and quickly launch clinical studies.
Researchers gain easy and automated access to data capture, sample tracking, data exporting and Exago custom reporting hosted in the OmniCloud™. The package also includes standard process workflow diagrams, a validation starter kit and a “quick-start” implementation schedule.
T1xpress capabilities include the following:
This prepackaged and fully hosted turnkey solution will allow for a much shorter implementation schedule, affording smaller clinics all the benefits of a tier I solution at a much lower total cost of ownership.
Anju is dedicated to the process of enhancing a patient’s quality of life by reducing the time to market of essential life-saving treatments.
Pharmaceutical, biotechnology, contract research organizations, diagnostic and device firms, and academic medical centers partner with Anju to maximize the value of their clinical research investments and to develop safe and effective healthcare treatments for patients.
The Most Intuitive EDC Suite on the Market
Featuring superior usability and flexibility, TrialMaster® is the EDC solution for Phase I – IV clinical trials
Proactive eSource and Early Phase Site Automation Solution
Bedside Data Collection (BDC) provides an automated solution to paper-based processes.
Interactive Response Technology
IRTMaster delivers powerful randomization methods combined with our fully validated and configurable trial modules.
Coding Clinical Data Against Medical Dictionaries
AutoEncoder is a modern and sophisticated tool for consistent and accurate coding out of the box.
Actionable Intelligence
Acuity is a powerful and flexible data aggregation, visualization and analytics platform driving actionable knowledge in real time.
Clinical Trial Management System
CTMS is designed to help sponsors and CROs overcome the technical challenges associated with managing clinical trials.
SAS based Report Software – FDA Submission capable
BioStats TLF (Tables, Listings and Figures) is a statistical authoring tool for creating the highest quality safety and efficacy tables, listings and patient profiles.