FeasiCon

FeasiCon (Feasibility Concierge) is a support system that enables the centralized management of feasibility studies to site selection for clinical trials and clinical research. The system allows the entire process—from survey requests to data aggregation and site selection—to be completed online. After the survey and trial implementation, site information can be stored in a database.Since English is supported, feasibility studies and site selection can be conducted both domestically and internationally.

Key features	Feature Overview	Benefits
Project Setup	Instantly track and visualize the status of your project inquiries and ongoing investigations.	Seamlessly track and manage your organization’s projects: Centralized oversight with instant access to historical insights. Advanced search capabilities by condition, status, and more. Exclusive access to detailed project info for assigned team members only.
Dynamic Survey Builder	Survey Design Studio: View and configure detailed survey information. Customize questions and response options based on research needs. Bulk registration and duplication of surveys. Create custom survey formats tailored to each organization.	Reduce the hassle of creating surveys from scratch each time.
Bulk Survey Distribution	Send bulk survey requests globally with error-checking and track response statuses in real time.	Enable real-time collaboration among project members while safeguarding against data breaches and document errors with a seamless, secure platform.
Streamlined Survey Completion	Seamlessly submit your survey responses with smart validation: only predefined answers are accepted, and incomplete mandatory fields prevent submission.	Prevent response errors and omissions with built-in validation.
Document Attachment	Easily attach documents along with your survey	Attach estimates directly to survey results for streamlined clarity.
Review and Aggregate Survey Results	It is possible to view the list of survey responses grouped by organization name.	All submitted survey results can be viewed in the system. Resubmission requests, resubmissions, and withdrawals can be completed within the system. The reasons for selection decisions can be recorded.
Trial Site Visit Scheduling	Scheduling Function for Site Visit Requirement Assessments	The system streamlines and centralizes the scheduling of site selection visits between pharmaceutical/CRO and SMO/trial sites, making the entire process efficient and seamless within the platform.
Language Toggle	Switch between Japanese and English	Feasibility surveys can be conducted both domestically and internationally.

Advantages of Use

Performance

・Proven success in implementing solutions with pharmaceutical companies and national healthcare institutions.
・Renowned for a user-friendly interface and exceptional post-implementation support.