Viedoc is a clinical trial management system designed to streamline research processes. It offers electronic data capture, patient recruitment tools, and customizable workflows. The platform provides real-time monitoring, audit trails, and reporting capabilities. Viedoc also integrates with existing systems, ensuring seamless data exchange and minimizing errors. This comprehensive solution supports efficient trial conduct and data quality.
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Viedoc is a web-based electronic data capture (EDC) system designed for clinical trials, allowing researchers to collect and manage study data efficiently.
Yes, Viedoc has an intuitive interface that makes it easy to use, even for users with limited technical expertise.
Viedoc is suitable for various types of clinical trials, including Phase I-IV studies, observational studies, and post-marketing surveillance studies.
Yes, Viedoc can be integrated with a range of other systems and tools, such as electronic health records (EHRs), clinical laboratory information systems (CLIS), and medical imaging platforms.
Viedoc follows strict security protocols to ensure that all study data is protected from unauthorized access, including encryption, firewalls, and role-based access control.
Viedoc provides comprehensive customer support, including online resources, user guides, and dedicated support teams to assist with any questions or issues.
Yes, Viedoc offers customization options to tailor the system to your organization's unique requirements and workflows.
Yes, Viedoc meets or exceeds all relevant regulatory standards, including 21 CFR Part 11, GDPR, HIPAA, and other global regulations.
Viedoc includes built-in features for data quality checks, validation rules, and automated reporting to ensure high-quality study data.
Yes, Viedoc is a cloud-based system that allows users to access their study data from any location with an internet connection.
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