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Overview

 

In a regulated or a non-regulated environment, one of the initial steps to streamline the quality procedures is to have a document management system in place. Some of the salient features of the product are defined below:

 

Manages documents efficiently.

Full-Text Indexing and Search .

Direct preview and editing of Files.
IMassive data import tool (Multiple Files + Sub-Folders).
Access Control Lists for Users and Groups.
Check-In / Check-Out, Version Control and preservation of previous revisions.
Data Commenting / Discussion.
Real-time logging of user activity.
Periodic File Archiving to external storage volumes
FDA 21 CFR part 11 compliance .

 

Technical Features

Web based secure system
Support multi-platform environment.


 
 
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