Why Choose Veracity Logic?

Our innovative VLIRT® system is a user-friendly, configurable, readily customizable Interactive Response Technology (IRT) platform developed to meet the needs of the clinical trial industry. For more than a decade, Veracity Logic has delivered customized IRT solutions to leading Pharma and Biotech companies internationally, with one of the best up-time records and in-study change rates in the industry. We offer strong functionality in a value-friendly package…with an emphasis on personal service! That’s why our 21CFRPart11-compliant system is the choice of dozens of Sponsors, CROs, and Clinical Suppliers.

We invite you to join the VL family and see for yourself…

IRT Features

  • Subject-Management
  • shipments
  • CTM
  • Inventory
  • SIte-Management
  • Data-Transfer
  • User-Management
  • User-Help
  • Validation

Get to know us…

At Veracity Logic, we’re as proud of our ability to manage the real-life demands of clinical trials as we are of our technology. We’ve built our business on four key principles—and the word is out!


We take a system from URS approval to release to Client Testing in four weeks. And during the trial, you needn’t wait eons for system modifications. Most changes to a project system can be completed in a matter of days, or complex system requests within two weeks.


Our IRT gets kudos from clients for flexibility, the ability to adapt to special project needs, not only at startup but for mid-course corrections as well. Our ease of configuration and customization surpasses that of many larger IRT providers in the industry.


A successful clinical trial means having vendors on your team who dive in as allies to meet project needs. At Veracity Logic, we’re not much on formality, just for rolling up our sleeves and helping clients find better ways to meet their IRT goals.


VLIRT®’s highly configurable, modular platform sits on fully validated CORE technology. That gives Sponsors and CROs two important advantages: less need for custom coding, and greater price flexibility, using only those modules required for the project.

See our latest Hot Topic:

Protocol Deviations: We need authorization…quick!


The study has been suffering from slow enrollment.  An excellent candidate, medically speaking, walks into Site 101 but there’s one problem: The minimum enrollment age for the clinical trial is 18. The age of the new potential candidate is 17 years, eight months. The Study Coordinator at the site not only needs a quick decision, [...]