Product Overview
Viedoc EDC helps users easily collect, validate and report on clinical trial data. With our browser-based interface, you can capture and manage data with greater accuracy and efficiency. We’ve made our EDC software flexible, effortless, and dependable, so you can focus on producing more accurate outcomes.
- Flexibility by design
Easily customized for each study setup per your protocol. - Effortless for every user
Designed for fast, intuitive clinical trial operation. - Secure and compliant
Mitigates security, safety or privacy concerns.
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
What export formats are supported?
Viedoc supports exports to Excel, ASCII, SAS, PDF, and CDISC ODM
Is Viedoc CRF 21 CFR Part 11 compliant?
Yes, statements of compliance with various regulations, including 21 CFR Part 11 and data privacy laws, are available upon request.
Does Viedoc store an independent contemporaneous investigator copy of the eCRF?
Yes, all versions of a form are stored at the time the form is saved, and these remain under the investigator's control.
Where and how frequently are backups performed?
Backups are taken, encrypted, and replicated to the paired Microsoft Azure region every five minutes. Additionally, a full backup for each instance is encrypted and transferred to cold storage at a third location, where it is read back, restored, and tested for integrity every 24 hours.
About the company
For two decades, we have perfected the craft of making clinical data more accessible so that greater discoveries can happen sooner.
At Viedoc, we believe in life and science, in people, and in our collective power to change the world and build a healthier future. That unmatched driving force is what pushes us to innovate, accelerate and improve every aspect of modern clinical studies.
Since 2003, Viedoc has united scientists and clinical trial professionals in a shared mission of pushing life-changing research forward. Our solution has been used to power thousands of studies, by collecting data from over a million patients and allowing it to flow smoothly across sites and countries. We take great pride in helping bridge the gap between patient and researcher—and, in the best of cases, between research and breakthrough.