What problems is Viedoc solving and how is that benefiting you?
Paper-Based Data Collection Issues
Traditional clinical trials relied on paper CRFs, which were slow, error-prone, and hard to manage.
Viedoc replaces these with electronic CRFs, reducing manual errors and speeding up data entry.
Data Fragmentation
Clinical trial data often comes from multiple sources (labs, devices, sites).
Viedoc consolidates all data into a single system, eliminating silos and enabling real-time access.
Complexity of Modern Trials
Increasing trial complexity and use of connected devices require flexible systems.
Viedoc offers customizable study setups and supports integrations for ePRO, RTSM, and external data.
Regulatory Compliance
Ensures compliance with FDA 21 CFR Part 11, ICH-GCP, GDPR, and HIPAA.
Provides secure, cloud-based storage with role-based access and audit trails.
Improved Data Quality
Built-in validation checks and real-time monitoring minimize errors.
Automatic query handling and SDV streamline data cleaning.
Faster Study Setup
Easy CRF design and deployment reduce timelines.
Users can program eCRFs themselves quickly without heavy coding.
User-Friendly Interface
Clean, intuitive UI makes navigation simple.
Highly customizable forms and workflows for different trial types.
Enhanced Collaboration
Supports multiple roles and sites with centralized access.
Integrated modules for randomization, supply management, and reporting.
Security & Reliability
Frequent encrypted backups and disaster recovery protocols.
Independent investigator copies of eCRFs maintained for compliance. Review collected by and hosted on G2.com.