They are typically based on picture archiving and communications systems (PACs) or research information systems (RIS), which were originally developed for the medical/ hospital segments and poorly reverse engineered to meet the requirements of the clinical trial segment which are substantially different.
In addition, most of the traditional options available to sponsors rely more on manpower rather than technology. This has resulted in solutions which provide very little control to the sponsors during the trial resulting in avoidable budget overuns, delays and risks to the trials.
The company and its products are built on the following
6 inviolable EIFCCT
fundamentals:
Efficiency
Innovation
Flexibility
Control
Comprehensive
Transparency
Deliver game changing solutions to simplify clinical image management in clinical drug and device development.
Radiant Sage's core belief is to give control back to the sponsor while managing clinical imaging trials. We believe that clinical trial outsourcing should not be at the expense of loosing control of the trial or the flexibility to selectively outsource certain components of the trial. The sponsor must have transparency throughout the trial process and have the flexibility to outsource or insource specific components of the trial.
We further believe that the greater the sponsor involvement in the development process, the more their learning and subsequent impact on design, execution and outcome.
Radiant Sage is focused on providing clinical image management solutions for the pharmaceutical, device, bio tech and research organizations involved in drug discovery and research. Our solutions are the only purpose built offerings available on the market today. They are Web 2.0 based offered under a SaaS delivery model providing full functionality of a core lab. The solutions have been specifically designed to enable sponsors to retain control of the trial without having to resort to expensive, time consuming, error prone and inefficient options available today.
We have developed our solutions based on a deep understanding of the imaging clinical trial process, FDA's regulatory requirements and the unfulfilled needs of the trial sponsor and various participants in the trials.
The solutions (Corelab-in-a-Box™ and RadVista Viewer) are designed to enable a sponsor to quickly set up a trial with custom or predesigned standard workflows as required by the protocol and begin collecting the required data within a few weeks. And all this can be done without having to invest in additional capital infrastructure using our SaaS delivery model. In addition, the sponsor has the option to manage the entire trial in-house using its own resources thus saving money and avoiding delays due to the long lead times required for identifying and, implementing the traditional out-sourcing options.
So, whether you are looking for a solution to run a small proof-of-concept trial or need to take control over the imaging data of a large phase 3 trial and integrate it into rest of the trial, Radiant Sage has the solution.
The Data Driven Innovation Award program was created in 2007 to recognize important vendor/sponsor relationships and to build awareness of new technology in the clinical data management field.
SCDM
2013
Radiant Sage, a provider of on-demand clinical trial image management solutions, today announced that it has received the Frost & Sullivan 2012 Customer Value Enhancement Award for its clinical trial image management solutions.
Frost and Sullivan
2012
Radiant Sage, a provider of on-demand clinical trial imaging infrastructure solutions, today announced that it has been named to CIOReviews list of 100 Most Promising Technology Companies. The CIOReview100 includes companies that are gaining momentum in the technology industry and making an impact.
CIO Review
2014