Role-based permissions protect sensitive study documents, ensuring only authorized users can view or manage files.

Secure, granular permissions tailored to each user.

All clinical trials documents right from Protocols to till final CSR (A to Z) are stored in one organized hub.

Retrieve documents securely from any location, boosting flexibility and productivity.

Automatic version control keeps teams aligned with the most up-to-date information..

Share files, collect feedback, and collaborate seamlessly without delays.

Every upload, edit, and deletion is logged for transparency and regulatory compliance.

Automated hooks streamline processes, saving time and reducing errors.

For tasks without automation, users can carefully review documents to ensure quality.

A balanced approach of automation and manual checks keeps information accurate and trustworthy.

Designed to meet industry standards, making audits and inspections straightforward.