TrialMaster®
Reporting

The Most Intuitive EDC Suite on the Market

TrialMaster not only makes it easy to get the data into the system, it also makes it easy to get the data out. Below is a sample AE listing that embodies some deceptively sophisticated logic:

software-screen
 

The listing joins the Adverse Events to the Demographics to include the patient’s age and sex, then compares the onset date to the patient’s first dosing date to determine if the AE was treatment emergent. The final column lists all the concomitant medications the patient was on at the time of onset. This logic is built as part of the study design and is made available at the user’s fingertips, for the whole trial, for a site, or for individual patients.

This same extended design capability allows the production of custom SAS datasets, which can include both the clinical data and operational data (such as query response times). The clinical data can also be mapped against any of the SDTM standards to produce submission-ready datasets. These facilities include the population of derived variables, such as “study day,” unit-of-measure conversion, pivoting of data to create questionnaire and lab domains, and the creation of supplemental datasets.

TrialMaster also supports the development of graphical dashboards using the adhoc query tool LogiXML. These dashboards can be assigned to specific user roles, so different types of users see different information. The assigned dashboards are then displayed on the homepage when the user logs on.

Your onsite clinical research team has one main job — caring for patients.

The TrialMaster Electronic Data Capture (EDC) solution makes it easier for doctors, nurses and other medical professionals to enter and manage their clinical trial data, thereby freeing up the maximum amount of time to care for patients. This ease of use for investigative sites, coupled with state-of-the-art risk-based monitoring (RBM) and analytical tools, means that life science companies can shorten the time to market for essential life-saving treatments.

Anju Software provides leading, strategic eClinical solutions for clinical trials around the globe.

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.

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

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TrialOne®

Proactive eSource and Early Phase Site Automation Solution

Bedside Data Collection (BDC) provides an automated solution to paper-based processes.

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IRTMaster

Interactive Response Technology

IRTMaster delivers powerful randomization methods combined with our fully validated and configurable trial modules.

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AutoEncoder

Coding Clinical Data Against Medical Dictionaries

AutoEncoder is a modern and sophisticated tool for consistent and accurate coding out of the box.

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Acuity Analytics

Actionable Intelligence

Acuity is a powerful and flexible data aggregation, visualization and analytics platform driving actionable knowledge in real time.

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ClinPlus CTMS

Clinical Trial Management System

CTMS is designed to help sponsors and CROs overcome the technical challenges associated with managing clinical trials.

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BioStats TLF

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.

MORE ABOUT BIOSTATS TLF

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