assisTek COVID-19 Virus - Read here.
The eSource Company
Have Questions? Contact Us Now LinkedIn twitter


| Overview | Experience

assisTek has over 18 years of experience in successfully delivering eSource solutions used to collect data, electronically, from patients and clinicians in clinical trials.

The assisTek team brings a history of superior performance, and an unequalled record of innovation to every trial.  assisTek’s focus continues to be based on delivering advanced solutions used to solve complex data management, data quality, and cost issues.   Study metrics indicate that assisTek systems and services are extremely reliable, highly preferred by patients and site staff, and produce exceptional data quality.  assisTek provides an array of technological solutions and services to support Phase I, II and III clinical trials all over the world.  Depending on the point of origin, one or more of assisTek’s modules may be fused together to support a specific study’s needs:

assisTek has earned a solid reputation in the clinical trial marketplace by delivering solutions used in over 150 trials, in over 35 therapeutic areas, while supporting 46 different languages in 40 countries.

assisTek has consistently leveraged new technologies to quickly deliver outstanding value to study teams.

assisTek is currently leading advancements in the clinical trial market by implementing Direct Clinical Data Capture, Patient eDiary and Electronic Outcome modules on Android touch screen devices.

Direct Clinical Data Capture

These new technologies offer a host of improvements over our competitors, including patient retention media features, data transfer using cellular 3G/4G networks, SMS text and email alerts, and customized web reports to dramatically improve compliance and safety monitoring.

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.

More Information

Quick Contact: Comments/Questions