Affordable Full-Service CTMS for Trials of All Sizes.

A comprehensive feature set and advanced web-based architecture make TrialVista® the most cost-effective CTMS solution available.

Cutting Edge Technology

The TrialVista interface and relational database are constantly updated, enabling users to take advantage of the latest technological advances.

The adaptable Intuit foundation allows for rapid deployment across any number of users — unlike older CTMS systems, which can take days to load onto a server (and require often arcane IT skill-sets).

It also allows the rapid dissemination of software upgrades, and enables every client to take advantage of modules and features created for other users' trials.

Ease of Use

TrialVista features many Windows-based techniques, such as right-mouse clicking, and a familiar web-based navigation system. External users can be using the system within hours of going live. User-friendly translates to less training, fewer support requirements and reduced expenses.

Instantaneous Implementation

TrialVista's deployment can be measured in days, not months. Because it's web-based, there's no need for implementation on individual PCs scattered between sites. And because updates are handled automatically at our end, there's always the assurance that every user has access to the most current version of the software.

All of which means clients can immediately begin realizing a return on their investment. With trials often costing tens of thousands of dollars a day, this can be a key factor in achieving commercial priorities.

Comprehensive Reporting

TrialVista gives users access to a wide range of reports, customized to their specific needs. With near instantaneous reporting, users can have the information they need when they need it.

Our vast array of standard reports is complemented by ad hoc reporting options, which allow users to access, consolidate and distribute exactly the trial data that's most important to them.

Remote Monitoring Component

TrialVista's remote monitoring tools allow for effective and efficient monitoring — an absolute necessity for any viable CTMS.

Our CRAs access any relevant trial and site data prior to a monitoring visit and can make updates in real time throughout the visit. This allows Project Managers and Lead CRAs to evaluate site visit data without the delay of a paper-based reporting system, which can often take weeks.

Errors are easily reviewed and corrected, further optimizing CRA time. Projects requiring multiple CROs can take advantage of TrialVista's standardized tools, which are easily implemented across third party vendors and eliminate the confusion of multiple management systems.

Compatibility

TrialVista interfaces with the latest technology solutions required in clinical trials, including Integrated Voice Response Systems, Electronic Data Capture and Clinical Data Management. Compatibility with the Microsoft Office suite and third party shippers' software can further centralize trial management from drug supply to timely investigator payments.

The ability to import data from these systems lets users create a real-time comprehensive view of trial progress. This ensures up-to-date reports and trackers for trial personnel.

Technical Support

ARG realizes the strain that older CTMS systems, and the requisite on-site support they entail, can put on client's IT infrastructure and bottom line

That's why we designed TrialVista to be a cost-effective alternative to local implementation and support staff. The entire infrastructure resides with ARG, and we're responsible for all upkeep and upgrades. And we provide unlimited technical support throughout the course of the trial, eliminating any worries about technology getting in the way of progress.

Value vs. Cost

Clients are faced with CTMS costs that can vary from hundreds of thousands to several million dollars. How can they know which one is right for them?

TrialVista makes the choice simple.

It provides the management tools inherent in a top-of-the-line CTMS, without the high price and support costs that keep them out of reach of smaller pharmaceutical or biotech companies.

Our license model allows for concurrent internal and external users with varying permission levels, customizable to the client's needs. Costs are significantly less than the named-user model, in which additional users and turnover rates can increase the price exponentially throughout the life of the trial.

Since it's a modular system, sponsors can purchase only the components they need for a particular study. And its architecture makes it easy to create and deploy custom modules designed to meet specific trial needs.