• 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 » StudyManager launches Reveal 3.3

StudyManager launches Reveal 3.3

October 11, 2011
CenterWatch Staff

StudyManager, a provider of clinical trial management software (CTMS) and electronic data capture (EDC) solutions, has released Reveal 3.3, with enhanced features that provide greater ease of use and performance for research sites, academic medical centers, and hospitals.

Based on customer feedback and StudyManager’s nearly 20 years in the field, Reveal 3.3 offers a number of key ease-of-use and productivity enhancements, including: study budget interface, enabling faster review of budgeted payables; a “next appointment” feature, which provides at-a-glance patient information, helping coordinators prepare for upcoming appointments; a capability allowing users to project and review patient visit “windows”, helping to improve protocol compliance.

“Software development in any industry, especially one with the complex business needs of clinical research, is dynamic,” said Alec Fishburne, VP of operations at StudyManager. “We’re proud of the close relationship we have with our customers, and value their product enhancement recommendations. Reveal 3.3 is the result of that ongoing collaboration, and the exciting challenge of collecting suggestions from a diverse base of research site clients – including small, independent sites, multi-site organizations, health systems and academic medical centers – and finding common ground for a product that maintains our mission of flexibility and simplicity, while continuously improving for everyone.”

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

  • SurveywBlueBackground-360x240.png

    Sites Name Tech Acceptance as Essential Factor in Selection of Sponsors, Survey Finds

  • TrendsInsights2023-360x240.png

    WCG Clinical Research Trends and Insights for 2023, Part Two

  • TimeMoneyEffort-360x240.png

    Time is Money and So Is Effort, Budgeting Experts Say

  • TrendsInsights2023A-360x240.png

    WCG Clinical Research Trends and Insights for 2023, Part Three

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