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    Features & Benefits Example
        Portability 7" Tablet only weighs 13 ounces, and fits easily into purses & small bags
  Instant Data Sharing Always connected (using Cellular Network) to allow study team instant access to critical data
  Multiple Language Support Can support multiple languages, as needed, based on study requirements (including Hebrew, Japanese, Indian and more)
  Highly Customizable Any event or episode can be recorded on the eDiary, based on study requirements
  Email & SMS Text Alerts Alerts can be issued to study team based on patient compliance or safety concern. Alerts & reminders can also be issued to patient to improve compliance and engagement.
       Accuracy Checks data upon entry for format, range, type and allowable values
  Completeness Ensures data fields are complete
  Consistency Data collection is consistent across all users and countries
  Quality Assurance Daily Events screen makes it easy for patient to review and update data before submission.
       Monitoring Costs Decrease Eliminate Source Data Verification
  No Data Entry from Paper Eliminate Transcription Costs & Errors
  Significantly Reduce Queries Lower Costs and Data Management Time
  Labor Costs Reduced No Printing, Proofing, Distribution, etc.
      Real-Time Quality Checks Question responses & Events entries are checked for completeness and compliance, before being saved.
  Real-Time Compliance Monitoring Daily Reports can be reviewed by SC to monitor compliance.
  Message Alerts & Media Updates (Patient) Messaging and media are used to engage the patient and improve compliance (including email, text, games, trivia, study status, and newsletters).
       Medical Standards Enforced (option) Undesirable events can be reported in real-time, and handled with appropriate intervention.
  Alerts Custom email or text messages alert staff immediately of potential safety events.
  Efficient Adverse Event Processing PI can be alerted (via email or text) regarding any potential AE
  Consistent Training Customized training modules enforce system understanding, before being granted access.

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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