ePRO-NOW™: Study Build Application

On-time, error-free ePRO configuration

ePRO-NOW FAQ

The ePRO-NOW™ Study Build Application is a revolutionary way to create on-time, error-free ePRO solutions for multiple platforms such as smartphone, tablet, web and sms.

A product of Arrowhead Electronic Healthcare's Reliability Engineering, ePRO-NOW™ was built to eliminate common points of failure in typical ePRO solutions including requirements errors, software programming errors, manual testing errors, translation errors, and project delays.

Key Functionality:

Study Design Module

  • Non-software programmers can build complete ePRO studies
  • Visual form design editor similar to Photoshop
  • Single system for smartphone, tablet, web and sms
  • Library of re-usable questionnaires, forms, buttons, and images
  • Easy-to-use logic editor suitable for most ePRO studies. Custom code interface for use in highly complex studies
  • Full language and locale capability
  • Press "run" at any time during the design process to operate a live web version of your ePRO solution
  • Generates validated code that creates real-time ePRO for Web. Code for smartphone and tablet is generated then loaded by Arrowhead onto devices

Study Specifications Module

  • Integrated study specifications module for efficiency and control
  • Export from web to .PDF
  • Screen flow diagram generation and exporting
  • Versioning and document control
  • Change log
  • Approvals

Software Testing Module

  • Automated code generation and library function eliminates the source of most configuration errors
  • Visual, run-time designer speeds up testing cycles
  • A virtual army of dumb monkeys test and document each possible navigation path
  • Automated generation of translation verification documentation

General Functionality

  • Web-based system for global collaboration and scalability
  • Easy-to-use navigation tree to help each team manage multiple programs, studies, questionnaires and forms
  • Authenticated access is provided to selected functionality based on rights and roles
  • Validated for regulatory requirements for use in global clinical trials