• SKIP TO CONTENT
  • SKIP NAVIGATION
  • Patient Resources
    • COVID-19 Patient Resource Center
    • Clinical Trials
    • Search Clinical Trials
    • Patient Notification System
    • What is Clinical Research?
    • Volunteering for a Clinical Trial
    • Understanding Informed Consent
    • Useful Resources
    • FDA Approved Drugs
  • Professional Resources
    • Research Center Profiles
    • Clinical Trial Listings
    • Market Research
    • FDA Approved Drugs
    • Training Guides
    • Books
    • eLearning
    • Events
    • Newsletters
    • White Papers
    • SOPs
    • eCFR and Guidances
  • White Papers
  • Trial Listings
  • Advertise
  • COVID-19
  • iConnect
  • Sign In
  • Create Account
  • Sign Out
  • My Account
Home » Oracle launches Central Coding Release 3.0

Oracle launches Central Coding Release 3.0

March 2, 2011
CenterWatch Staff

As the volume of clinical trial data continues to grow, consistent coding and normalizing of data across multiple trials is imperative in advancing the effectiveness and efficiency of clinical trials.  To this end, Oracle has announced the availability of Oracle Health Sciences Central Coding Release 3.0. 

The new clinical trial data coding and dictionary management application includes expanded query management and automated workflows that help clinical trial sponsors and CROs improve the efficiency and consistency of the coding process.

The new release also features enhanced integration with Oracle Health Sciences InForm Global Trial Management Global Trial Management system, and a flexible, multilingual application that automates coding and minimizes the manual effort required to code verbatim terms. It is the first coding solution to be certified by the Uppsala Monitoring Centre, the World Health Organization collaborative center for international drug monitoring.

Oracle Health Sciences, based in Redwood Shores, Calif., collaborated with multiple users in the clinical trial community on this latest release, soliciting feedback from users to deliver a more comprehensive and widely-tested product.

“Consistent coding is fundamental to normalizing data for analysis and regulatory submission, but it’s no easy task in today’s complex, global research environment,” said Neil de Crescenzo, senior vice president and general manager, Oracle Health Sciences.  “Integration is critical to achieving the necessary workflows to efficiently code across multiple trials in multiple languages.”

 

Upcoming Events

  • 16Feb

    Fundamentals of FDA Inspection Management: Reduce Anxiety, Increase Inspection Success

  • 21May

    WCG MAGI Clinical Research Conference – 2023 East

Featured Products

  • Spreadsheet Validation: Tools and Techniques to Make Data in Excel Compliant

    Spreadsheet Validation: Tools and Techniques to Make Data in Excel Compliant

  • Surviving an FDA GCP Inspection

    Surviving an FDA GCP Inspection: Resources for Investigators, Sponsors, CROs and IRBs

Featured Stories

  • Revamp-360x240.png

    Califf Calls for Major Evidence Generation Revamp, Experts’ Opinions Differ

  • AskTheExpertsGreen-360x240.png

    Ask the Experts: Managing Investigational Products

  • SurveywBlueBackground-360x240.png

    Survey Outlines Site Challenges, Successes on Diversity

  • PatientCentricity-360x240.png

    Site Spotlight: DM Clinical Shows Patient Centricity Doesn’t Have to Break the Bank

Standard Operating Procedures for Risk-Based Monitoring of Clinical Trials

The information you need to adapt your monitoring plan to changing times.

Learn More Here
  • About Us
  • Contact Us
  • Privacy Policy
  • Do Not Sell or Share My Data

Footer Logo

300 N. Washington St., Suite 200, Falls Church, VA 22046, USA

Phone 617.948.5100 – Toll free 866.219.3440

Copyright © 2023. All Rights Reserved. Design, CMS, Hosting & Web Development :: ePublishing