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
Study data can be collected in TrialOne from offices, hospitals and universities throughout the world by physicians, nurses and clinic staff using TrialOne’s proactive real-time, browser-based system. Data collection can take place at a patient’s bedside or in the examination room using tablets and other handheld devices such as mobile phones and mini barcode scanners. The clear and intuitive data collection screens provide a responsive and user-friendly method of collecting the information that is most important for your clinical trial and business.
With TrialOne, the site can electronically confirm volunteers into visits by scanning subject barcodes and start collecting data immediately. The site team can connect directly to medical devices for immediate and accurate results without the need for double data entry. TrialOne enables researchers to scan barcodes to verify the correct specimen container is being used or the correct dose is being given, and to record the collection time with a hands-free USB-attached foot switch.
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.