Discover the Power of Online Feasibility for Trial PlannersRequest a Demo
Modern web technology has changed how people relate to information and others.
For example, online platforms make finding just the right restaurant, hotel, or flight more convenient than ever. And social networks make establishing relationships, without regard for geographic and organizational boundaries, easier than ever.
Shouldn't trial planners be able to find key feasibility information and establish relationships with research centers just as easily?
We thought so.
OF FEASIBILITY QUESTIONS
1,166,000 trials at site-level
59,000 institutional profiles
1,400 epidemiological databases
67 diseases with feasibility instrument
69 diseases with patient mapping
>80% of clinical trial collaborations
The ViS platform is transforming the feasibility process for trial planners using the same web technologies that have transformed the consumer web.
Trial planners are using ViS to:
Find the best locations
Streamline the feasibility process
Engage with research centers
ViS provides trial planners with an unparalleled feasibility experience:
Seamlessly navigate customizable feasibility analytics and visualizations worldwide using an integrated platform.
Closely evaluate research centers using extensive center profiles, without the need for cumbersome questionnaires.
Manage the entire feasibility process, including your direct engagement with research centers, from one central location.
The ViS platform has a range of robust capabilities, which are summarized below. Click a capability to explore it in more depth.
Seamlessly navigate across a range of feasibility analytics and visualizations
Extensively evaluate and compare centers across the globe
Quickly determine the aggregate capabilities of research center networks and access their shared infrastructure
Extensively evaluate and compare both general and disease-specific investigator information
Get advanced filtering capability and/or assistance from ViS experts
Organize and manage research center evaluation and communication at scale
Create disease-specific networks that consolidate analytics about centers and investigators engaged with your organization
ViS integrates information from three primary data sources, through collaborative analytics:
Research centers and investigators
3rd party data
ViS analytics are built and continuously updated using a three-step process:
Globally distributed clinical research analysts use parsing algorithms, natural language processing, and pattern recognition to capture and curate data from thousands of sources.
Information is continuously harmonized and integrated using proprietary semantic technologies to generate geo-referenced disease-specific analytics from country down to research center level.
Analytics are continuously validated and enriched by regional clinical research experts and further integrated with inputs from the research centers.
Trial planners can use the ViS platform according to the suggested workflow:
Choose location based from country to postal code level worldwide, based on disease-specific filters
Use the visualizations showing the comparative analytics of locations to find centers and/or investigators that are most attractive
Select centers/investigators and create lists for further evaluation
Review center/investigator profiles to determine if their capabilities meet your requirements
Invite the preferred centers to be part of your network and engage further
The number of Alzheimer's research centers in a country
HIV recruitment research centers in a state
Breast cancer cases in a city
Diabetes investigators in a postal code