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The eSource Company
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Investigator can review immediately after email notification of new or updated Adverse Events
Easy text entry with onscreen keyboard
Custom features accessible from Main Menu (access based on user type and security level)
Select ConMeds, Non-Drug Therapies from pre-populated, easy scroll list. Avoid written mistakes!
Jump to patient’s history to review data recorded during earlier visits.
Graphical display of patient's vital sign history
Record Study Coordinator Follow-up
Easily review AE History and take action
Close ongoing ConMeds by accessing ConMed history

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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