The eSource Company
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    Features & Benefits Example
   
SYSTEM
     Patient Reported Outcome   Multiple Language Support A device at one site may support more than one language (including Japanese, Hebrew, Indian, and more)
  Exit/Save/Resume Allow patient to Exit, Save, & Resume during long visits with many questionnaires
  Instant Data Transmission Allows study team to immediately review entries, track patient progress, etc.
  Large, bright, crisp screen Easy to see buttons/images, read text, and use Tablet, regardless of experience and age.
  Supports varying requirements for different site visits The system can support varying questionnaires based on site visit, etc.
   
IMPROVED DATA QUALITY
      Accuracy Checks data upon entry for format, range, type and allowable values
  Completeness Ensures data fields are complete/questions are answered
  Consistency Data collection is consistent across all users and countries
   
COST SAVINGS
       Monitoring Costs Decrease Eliminate Source Data Verification
  No Data Entry from Paper Eliminate Transcription Costs & Errors
  Significantly Reduce Queries Lower Costs & Study Team time
  Labor Costs Reduced No Printing, Proofing, Distribution, etc.

Improve Critical Study Objectives

  • Patient Compliance
  • Patient Engagement
  • Safety Management
  • Data Management

Learn more about improving key aspects of your study. More Information

eSource In Clinical Trials | Support FDA Guidance

According to the FDA guidance on source data in electronic form, eSource will help to eliminate unnecessary duplication of data, reduce the opportunity for transcription errors, promote the real-time entry of electronic source data during subject visits, ensure the accuracy and completeness of data, and more.

assisTek's TotalSource solutions capture these improvements to source data, and are customized to each individual protocol. More Information

Company Overview

assisTek successfully fuses new developments in mobile technology with creative software solutions to revolutionize the collection of data from patients and clinicians in clinical trials. We have proudly been helping clinical trial teams achieve success for over 18 years, in 40 countries with 46 languages. Our expertise can support studies in any phase.

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