The essential EDC software
Streamline your clinical trials while making each user’s activities and tasks easier, faster, and more enjoyable
Streamline your clinical trials while making each user’s activities and tasks easier, faster, and more enjoyable
With the increasing demand for accessibility, flexibility, and speed in clinical trial management solutions, it’s no wonder more and more major companies are turning to Viedoc—and staying with us.
Thanks to minimal setup time and maximal ease of use, you and your clinical trials can benefit from Viedoc more or less instantly.
Viedoc's EDC software allows you to efficiently access, manage, review, and share clinical trial data—from any device, at any time.
"It is easy to navigate all the features for a site user on the clinic page. All the functionalities are available on separate tabs, be it SDV, Sign, Clinical Review or Data Review, and can be easily noticed in the UI."
Manu R.
Data Manager Research
"I have been using Viedoc for almost 8 months now. I've felt that Viedoc is more user friendly compared to other EDC's I've seen or worked on."
Ananthu A.
Associate Analyst
Data collection
Features for collection, viewing and reviewing of CRF data in an ICH GCP compliant manner, including capture of binary data (images / documents)
Sign data on form, visit or patient level Link data between forms (e.g. AE and CM)
Laboratory reference values with time, location and factor scope
Study building
Drag-and-drop form design with more than 18 different item types to choose from
Form preview allowing the designer to verify layout, conditions and checks directly onscreen
Automatic creation of blank and annotated CRFs
CDISC CDASH form library with over 20 ready-to-use forms
Ready-to-use study templates in CDISC ODM XML format
Form translator for managing multiple study languages
Best-in-class support for complex study designs / requirements
Study management
Role delegation service
Study level database lock feature
Study-recreation from a previous snapshot (CDISC ODM)
Unique and fully self-service study decommissioning feature including status reports and archiving recommendations
Documentation and certification management
Assignment of study designs
Study settings
Study license management
API management
TMF management
RTSM management
Reference data management
Medical coding dictionary management
User management
Site creation, with code, time zone, type (production / training), recruitment metrics
User management, with invites, resets, and removals
An integrated and configurable ePRO / eCOA feature according to the BYOD model
Supports custom workflows and complex decision trees Televisits
Reminders in local language via SMS and email Customizable VAS
File upload
Drawing pad with body map, signature line, or blank background
Support for unscheduled data entries
40 languages including righttoleft typing
Library of validated ePRO / eCOA forms
Integration with smartwatches, thermometers, scales, and more
Coming soon. Our eConsent process is smooth and reliable. Once combined, our range of products deliver an enhanced user experience with maximum flexibility for both the site and the participant. Remotely share essential information with participants and assess their understanding, expedite participant identification, and retrieve signatures.
Secure peer to peer video calls
Screen sharing
No installs or downloads
Easy access
Join in one click
Audit log tracking date, time, duration and participants
24 / 7 output to Excel, CSV, SAS, PDF / A (compliant to FDA submission, eCTD) and CDISC ODM formats
Scheduled exports
Online data preview and chart visualization
API for import and export of data in CDISC ODM
Real-time metrics on data quality and performance
Set up your study, manage sites and user roles, and close everything once you’re done—without having to go through a helpdesk or tech manager.
"The system is incredibly robust and is very user friendly, both to sponsor level satff, as well as site staff who remotely enter data."