Viedoc

Streamline Clinical Trials with Viedoc – Advanced Software for the Life Sciences Industry

Viedoc stands as a leading tool in the Electronic Data Capture (EDC) Software category, offering a modern and intuitive platform tailored for clinical trial management. Designed to accelerate clinical research, it helps pharmaceutical, biotech, and medical device companies, as well as research institutions, securely collect, validate, and analyze study data. Since its inception in 2003, Viedoc has powered studies involving over 1 million patients across 75+ countries.

Why Use Viedoc?

Viedoc excels in clinical research management through:

• Comprehensive Study Support: Its eCRF feature facilitates the creation and management of electronic case report forms, audit trails, smooth data capture, and study randomization. This ensures compliance with regulatory standards like 21 CFR Part 11.
• Streamlined Data Management: Powered by cloud security, role-based access, and simplified data export features, Viedoc centralizes and streamlines clinical trial data management.
• Customizable and Scalable Design: Users can easily design trial-specific workflows and edit checks while reusing templates to save time during study builds. Its simple-to-navigate validation and coding systems make programming efficient and user-friendly.
• Intelligent Reporting and Documentation: Viedoc ensures real-time reporting functionalities and a robust documentation system for better operational performance and oversight during studies.
• Regulatory Compliance and TMF Tools: It enhances inspection readiness with pre-built regulatory adherence models and customizable role permissions, facilitating audits and maintaining a compliant trial framework.

Who is Viedoc For?

Viedoc caters to a diverse spectrum of users, including:

• Sponsors and CROs: Pharmaceutical, biotech, and medical device firms benefit from Viedoc’s advanced tools, ensuring efficient data management and compliance.
• Clinical Researchers: Research institutions leverage Viedoc’s user-friendly interface and streamlined documentation to effectively manage trials.
• Study Designers: Designers can take advantage of its flexible eCRF builder and content workflows for personalized and scalable study setups.
• Data Managers and Monitors: Professionals in clinical data management and monitoring rely on features like centralized data access, audit trails, and role permissions for maintaining data integrity.

In conclusion, Viedoc provides a robust, reliable EDC system that simplifies complex clinical trial operations. Whether for designing trials, managing data, or ensuring compliance, Viedoc empowers its users to focus their efforts on innovation and quality research while leaving trial execution and management to its capable platform.