Velos eResearch

Clinical innovation takes place when you have more time.

Velos eResearch is the most comprehensive and adaptable clinical research management suite (CRMS) available for automating all administrative, financial, and research activities.

Designed to promote productivity and efficiency, Velos eResearch simplifies the management of the entire clinical research portfolio by linking study status, patient enrollment, calendars, budgets, electronic data capture and more.

Top Ten Reasons Why Customers Trust Velos eResearch

  • Fast setup and turnaround time
  • Excellent data quality
  • Extensive standard libraries
  • More accurate and comprehensive research billing
  • Better revenue recognition
  • Greater grant and research capacity
  • Support for multiple technologies and vocabularies
  • Easy integration with 150+ systems
  • HIPAA and 21 CFR part 11 compliant
  • 24/5 customer support available for all products

Tailored to customers’ present and future needs, Velos eResearch is

  • the largest commercial system available in the CTSA community
  • a scalable system that supports end user diversity for successful enterprise adoption
  • an innovative solution for advancing patient-centered care and translational research

Velos eResearch Features:

Unleash the Power of Data with Velos eResearch


Compliance is complex, but the approval process can be simple.

  • Build online protocols
  • Ensure procedures follow protocol specifications
  • Easily manage consents, IRB reviews, regulatory documents
  • Manage multiple sites and receive data from across the globe
  • Set security and user permissions

Dartmouth and Norris Cotton Cancer Center use an integrated CTMS to enhance compliance.


Efficient patient management is doing the right thing at the right time.

  • Create interactive, detailed study and patient calendars
  • Track studies from approval to close-out
  • Streamline patient registry, scheduling, monitoring, and follow-up
  • Record visits, get timely notifications, and reduce deviations

Big payoffs for The University of Michigan and University of New Mexico.


Budgeting is telling your money where to go before it leaves your bank.

  • Check the financial feasibility of each study
  • Ensure prompt, accurate invoicing
  • Reduce improper billing and get paid for each completed task
  • Track current revenue and forecast anticipated revenue


Compliant EDC is a friend of quality data and an enemy of double entry.

  • Develop Configurable Case Report Forms
  • Robust data query engine and reusable library systems
  • Central repository for documentation and safety plans
  • Site and study statistics
  • Adverse events alerts and outcomes reporting

The National Cancer Center of South Korea uses EDC to conduct 115 clinical trials successfully.


Frees you from the drudgery of bulk manual filing.

  • Continuous monitoring to identify changes and reduce compliance risk
  • Centralized location to manage multiple CDMs
  • Better version control
  • Significantly raise data integrity

An add-on module, CDM-R improves workflow automation, minimizes data errors, and maximizes revenue.


Information becomes power with the industry’s most advanced reporting solution.

  • 100+ out of the box reports
  • Create unlimited ad-hoc queries
  • Improve information accuracy
  • Effortlessly share reports with study teams, groups, and organizations

Cancer Trials Australia (CTA) creates custom reports to improve information accuracy.