edcpro
is a web-based alternative to traditional paper-based data
capture. It uses as its foundation a customizable template
applicable to all 4 phases of clinical studies, patient
registries and chart review trials in a large range of therapeutic
areas.
edcpro
effortlessly creates custom electronic Case Report Forms
(eCRFs) that mirrors paper-based Case Report Form (CRF)
design. Inherent real-time data validation provides instantaneous
feedback to ensure the integrity of your clinical study
data. Online reporting tools (status reports, customizable
database searches, etc.) provide the user with convenient,
up-to-date information on all aspects of the clinical study.
The end product is a powerful data-collection tool that
is clean, intuitive and user-friendly.
edcpro
is a robust, user-friendly secure environment that works
with any standard internet browser and is compliant with
all aspects of FDA 21 CFR Part 11
Sept 21, 2005 White Paper on edcpro2.00 available upon requestmore>>
Thursday,
Nov 3, 2005 edcproWebinar to launch release of v3.00. Please contact
us to register. more>>
Spring
2006
2-day Seminar on novel trial design for biotech - includes
demo of edcpro
3.00 more>>
