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.
CLICK HERE FOR DEMO
(This requires pop-ups to be enabled, if not, just click on the link while holding
down the Ctrl key)
*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