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LIMS Features

Laboratory Document Management: Centralize All Your Quality Documentation

All your quality documentation, linked to the right record and accessible in seconds during your audits.

Value for money
4.8
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Logo Bonduelle
Logo Leroy Merlin
Logo Decathlon
Logo BESIX
Logo EDF
Logo Onet
Logo Arthur Bonnet
Logo Guerlain
Logo Harman Kardon
Thanks to Excel file extraction, we filter and sort in one hour the elements we want to see appear. Based on this, I have a complete audit. I have access to all information and all documents are accessible through AQ Manager.
L.D.
Quality Manager - UCLouvain

Why Choose Our LIMS for Your Document Management?

All your laboratory documentation, accessible from the bench as well as from the office.

Ensure complete traceability

Each document, test report, protocol, or safety and equipment sheet, is timestamped and electronically signed (for test reports, analysis bulletins, and certificates of conformity).

Save Time Daily

Documents are accessible without having to search through multiple network folders or binders. Validations, distributions, and updates can also be automated.

Reduce Document-Related Errors

Reduce the risk of using an obsolete procedure, an unvalidated method, or incomplete information.

Capitalize and Preserve Knowledge

All your documentation is accessible and centralized, even during team changes or employee departures.

Benefits

How Does Document Management Work in Our LIMS?

Associate the Right Documentation with the Right Record

Our document management tool allows you to associate any type of document with any record in the application. For example: technical sheets and photos to your products, procedures (Word, PDF, etc.) to your methods, templates, and analyses, calibration procedures to your laboratory equipment, photos and documents to your collected samples, price quotes to your supplier purchase orders, etc.

Master Categories, Versions, and Deadlines

Classify your documents by category, track their versions, and define the language as well as validity dates. AQ Manager automatically alerts you of revisions to be performed at the due dates specified in each document.

Create Your Own Documentation from the Application

Create documentation directly in the application: add a URL link or file path, upload a file, or generate a new document via the integrated editor (PDF, Word, or Excel).

Access Your Documents via the Mobile Application

All your documents are accessible from the AQ Manager mobile application. Enrich the content by directly associating photos for metrology (before/after), diagrams, reports, or attached documents.

Authorizations, User Access, and Document Security

Define precisely who can view, modify, or delete each document. Your sensitive data remains protected, and each action is tracked and timestamped to ensure integrity and traceability.

Trustpilot

They chose AQ Manager LIMS

The great flexibility of customization of AQ Manager LIMS, which allows it to be effectively adapted to internal processes and specific user expectations.
Julien D. Product Manager – Chemical Sector
Are you interested in our laboratory software?

Test it for yourself!

With AQ Manager, benefit from tailor-made support, from demonstration to installation, with our team always by your side.
Our LIMS software solutions in figures
1450
supported companies
30
years of expertise
35
countries covered
+10 000
unique users per month

Discover all the features of our LIMS to optimize your laboratory management

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Frequently asked questions

A LIMS (Laboratory Information Management System), or laboratory management software, centralizes and automates the management of samples, analyses, results, and equipment. It ensures traceability of all operations.

A LIMS also integrates a document management module that links each procedure, operating method, or test report to the right record. This ensures traceability, meets accreditation requirements such as ISO/IEC 17025, and ensures that each team works on the latest validated version of a document.