TrialMaster
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Easy to Use

Unlike traditional software applications requiring special hardware and a team of developers and programmers to update and maintain them, TrialMaster runs over the Internet - like a series of specialized websites customized to the requirements of your specific clinical trial and workflow processes. The TrialMaster application does not require sponsors, investigator sites and other application users to install software or purchase special hardware. All you need is a PC or laptop, Internet Explorer 5.0 or better, a connection to the Internet, and a password. Just log in and the rest is simple and intuitive; training on the application generally takes no longer than 1 hour.

Here's how it works: (click on the screen shots to view enlargements)

1) Login/Password screen - Access to TrialMaster is protected by this Login/Password feature. Each individual requiring access to trial data will have his/her own Login/Password that allows access to specific trial information determined by the trial sponsor.

   

2) Trial Manager Menu - This menu allows the sponsor to enter information (name, address, e-mail address, login/password, etc.) regarding all TrialMaster users and associated sites. The status of each Internet case report form (iCRF) is available for viewing and the data export feature affords instant access to data. The Form Status Notification tool is a powerful e-mail communication sub-system that provides instant notification to all trial sites concerning adverse events, iCRF status changes and other important information. Trial reports are plentiful and are customized to client requirements.

   
3) Study Site Setup & Study User Information - These sections are accessed from the Trial Manager menu and make it easy to enter site and investigator information.
   

4) Investigator and Clinical Research Associate/Monitor Menus - Using these easy-to-navigate menus, investigators and monitors have access to trial information specific to their sites. For example, a monitor may access only those iCRFs that are being completed by their assigned investigators. A copy of the protocol may be accessed from this menu in a "word-searchable" format affording a convenient resource for investigators and monitors.

   

5) TrialMaster Reports - OmniComm has developed approximately 20 standard reports and is capable of producing custom reports to satisfy all needs. The reports provide real-time trial data analysis and can be printed for ease of distribution.


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