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Target e*CRF® - EDC Made Simple™

Target e*CRF® is a web-based, proprietary, data and project management system designed for ease of use and high throughput. Target e*CRF® has been used exclusively by Target Health Inc. since 1999. It is 100% accepted by sites and has been used as the “source” CRF. As a full service CRO representing over 20 companies at the FDA, we understand what it takes to run a trial. Target Health developed this software to streamline the process and optimize results.

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*For first time users, please click above and register; username and password will be emailed to you.

CLICK HERE FOR VIDEO TUTORIAL
DOWNLOAD DATA SHEET

Benefits include

  • Built in workflow enables intuitive set-up and execution.
  • Client can run in any environment
    • ASP hosted by Target Health or installed in-house
  • Fast set up and training (days, not weeks)
  • Proven
    • Over 100 studies completed
    • Over a dozen approved products on the market today which used Target e*CRF® for the pivotal trial(s)
  • Elimination of traditional paper CRF's
  • Minimization of data transcription and logic errors
  • Ability to use as the “source” CRF
  • In most cases, clients lock database within 1 week of LPLV (last patient last visit)

How We Differ!

  • Every object is re-usable
    • Once you set up a standard, or if you use CDISC, that can be enforced throughout
  • Comes configured with a “standard” database
  • Ability to generate web CRF and automatically print with SAS variables (annotated CRF)
  • Built in query management / edit check system
    • No programming required for edit checks
    • Can import edit checks directly from SAS
    • Client (or Monitor) can decide when edit checks are fired (upon data entry or batch)
  • Training
    • Sites trained in less than a day
    • Users trained in 2 days
  • Automatically provides E-mail notifications based on logic you define (also programmerless)
  • 100% accepted at sites
  • Ad-hoc reporting
  • Customized management reports
  • Built in Adverse Event Reporting
    • Generate standard safety reporting forms
  • Entire system (Study setup and configuration as well as data entry) can be run over dial up connection
  • Managing protocol amendments in hours (NOT weeks)
  • Modifying edit checks in hours (NOT days)
  • Managing patient enrollment
  • For Sites :
    • Allow sites to have more control
    • They can add/modify/register users
    • Monitors can better manage sites
  • Target e*CRF Newsletter™
    • Automatically generated from database (weekly, monthly, etc.)
    • Provides key information / graphs to sites
    • Keeps sites informed
    • Helps sites be competitive on enrollment, as they see where they stand relative to all sites involved in the study
    • Helps sites manage study progress – often used at site internal staff meetings