Real World Electronic Data Capture
Contact
CDISC
  • Home
  • The Real World solution
    • eCRF Build Options
    • Phase 4 Specialist
    • SaaS
    • How It Works
    • Our Products
  • Why We're Different
    • Cost Savings
    • Easy Setup
    • Quality & Compliance
    • Multi-lingual
  • Testimonials
    • Case Studies
  • About
    • White Papers
    • Management
    • News & Research

About CTEP: the creators of RealWorld EDC

Contact us

Real World EDC has been specially developed for observational studies.

Key features of the Real World EDC solution are that it is:

  • Flexible: Real World EDC can be rapidly customised for each trial and scaled to match your needs
  • Compliant: Our Real World EDC solution is CDISC-certified (Operational Data Model / ODM) and is designed to comply with the latest industry and regulatory requirements –FDA’s CFR 21.11 and ICH GCP guidelines
  • Supported by experience: Our expert team can build, validate and support your study
  • Study Builder: Alternatively, you can use our self-build tool to take control of the eCRF development process

To learn more about how Real World EDC can meet your observational study requirements contact us»

  • eCRF Build Options
  • Phase 4 Specialist
  • SaaS
  • How It Works
  • Our Products
  • Home
  • The Real World solution
  • Why We're Different
  • Testimonials
  • About
Learn More
or tell us about your project»
  • Clinical Trial EndPoint (CTEP) Ltd.
  • United Drug House, Magna Business Park,
  • Citywest Road, Dublin 24, Ireland.
  • Phone: +353 1 4637723
  • Fax: +353 1 4637785
  • Web: www.realworldedc.com

Legal Statement Copyright 2011 CTEP. All Rights Reserved.
Web Design by morsolutions