Qualsys provides an advanced and secure electronic trial master file management solution. Clinical trial companies use Document Manager for:
- Providing staff throughout the world a single system to input into, access and manage the same repository of information
- Traceability, control of ownership and responsibility management
- Advanced and automated reporting, data visualisation and dashboards to see how you are doing against the plan
Qualsys manages the implementation of our software. Our best practice framework helps configure the solution, train your super users and set up your system for lasting compliance and quality success.
Control any document
Document Manager enables you to control any type of document. This means you can control technical files, data, and pdfs. Document Manager is also compatible with CAD viewing technologies.
Employees are able to check-out documents for use in Microsoft Word, Excel and PowerPoint, safe in the knowledge that Document Manager is recording all the required compliance requirements in the background.
Control document types
Document Manager provides unshakeable control over who can access, change, update or approve a document is fit for purpose.
The software is incorruptible. The system offers a full audit trail and version history for each document, including those which have been archived.
Equipment acceptance testing
Audit Manager provides evidence of compliance with processes and equips you with foolproof mechanisms to eliminate process issues. You manage any type of audit or inspection activity, creating and storing checklists of questions ongoing use and analysis.
Integrate with Clinical Management System
Integrate with the other modules for a complete management system.
Read about our five phased approach to computerised systems validation.
Download our culture of quality toolkit for tips, advice and steps to building a true culture of quality.