Your dependable suite of eClinical solutions
On-demand expertise when you need it
Flexible, intuitive, and secure EDC management system
Easily capture data directly from study participants
Enable more productive video interactions
Document every study with precision
Streamline study record sharing with personnel and participants
Electronic signatures with full regulatory compliance
Flexible randomization for reliable study outcomes
Streamline and secure your clinical trial logistics
Medical coding that saves time and increases accuracy
Fulfil all requirements for PMS studies in Japan
For streamlined system integration
Technical expertise and support whenever you need it
Quickly achieve study design expertise
End-to-end expert study builds
Keep your Viedoc solutions running smoothly
Dedicated support and guidance for your studies
Including any planned Televisit using Viedoc Connect.
Excluding ePRO/eCOA forms managed in Viedoc Me.
It is mandatory that all applicants for the Accelerating the SDGs: Viedoc Free License Initiative attach a study protocol for verification. Applications without a study protocol are not qualified for the offer. An NDA will be put in place prior to protocol review by the Viedoc team.
Please check the correctness and completeness of the information below before sending the request.