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Overview

vDocument is a cutting-edge web application designed to enhance document sharing and collaboration between sponsors and stakeholders. With a focus on precision, security, and compliance, vDocument streamlines the process of sharing critical documents for view purposes.

Key Features

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Effortless Document Sharing

Effortless Document Sharing

vDocument simplifies the exchange of documents by providing a user-friendly interface for sponsors. Whether it’s clinical trial data, regulatory submissions, or project reports, vDocument ensures seamless access for authorized users.

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Assignment-Based Access

Assignment-Based Access

Sponsors can securely view documents relevant to their specific assignments. This targeted approach ensures that stakeholders only access the information they need, enhancing efficiency and confidentiality.

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21 CFR Part 11 Compliance

21 CFR Part 11 Compliance

vDocument adheres rigorously to regulatory standards, including 21 CFR Part 11. This compliance ensures data integrity, electronic signatures, and audit trail capabilities, making it a trusted solution for regulated industries.

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Zero-Level Audit Trail

Zero-Level Audit Trail

Every interaction within vDocument is meticulously recorded. From document access to annotations, the audit trail provides transparency and accountability, allowing sponsors to confidently navigate compliance requirements.

Why Choose vDocument?

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Security

Safeguard sensitive data, ensuring sponsor confidence in document sharing.

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Efficiency

vDocument accelerates sponsor-stakeholder communication, reducing delays and enhancing project timelines.

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User-Friendly Interface

Intuitive navigation and responsive design make vDocument accessible to users of all levels of technical expertise.

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