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Discover the Power of Online Feasibility for Trial Planners

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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.





148,400 trials

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.

ViS Capabilities

The ViS platform has a range of robust capabilities, which are summarized below. Click a capability to explore it in more depth.

Location Feasibility

Seamlessly navigate across a range of feasibility analytics and visualizations

Center Feasibility

Extensively evaluate and compare centers across the globe

Network Feasibility

Quickly determine the aggregate capabilities of research center networks and access their shared infrastructure

Investigator Feasibility

Extensively evaluate and compare both general and disease-specific investigator information

Advanced Analytics

Get advanced filtering capability and/or assistance from ViS experts

Feasibility Management

Organize and manage research center evaluation and communication at scale

Private Networks

Create disease-specific networks that consolidate analytics about centers and investigators engaged with your organization

ViS Approach

ViS integrates information from three primary data sources, through collaborative analytics:

  • Internal research

  • 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.

ViS Workflow

Trial planners can use the ViS platform according to the suggested workflow:

Step 1
Choose location based from country to postal code level worldwide, based on disease-specific filters

Step 2
Use the visualizations showing the comparative analytics of locations to find centers and/or investigators that are most attractive

Step 3
Select centers/investigators and create lists for further evaluation

Step 4
Review center/investigator profiles to determine if their capabilities meet your requirements

Step 5
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