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QUMAS

Cork, Ireland · Information Technology

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Last verified

May 2026

#electronic document management

#process management (compliants

#capa

#deviation

#change control

#audit)

#gxp compliance management

#quality management

QUMAS is a leading provider of Quality and Compliance Management Solutions for the Life Sciences industry, headquartered in Cork, Ireland.We specialize in delivering robust software solutions – including the QUMAS Compliance Platform – that help global pharmaceutical, biotechnology, and medical device companies navigate complex regulatory landscapes and maintain operational excellence.

Overview

QUMAS is a leading provider of Quality and Compliance Management Solutions for the Life Sciences industry, headquartered in Cork, Ireland.

We specialize in delivering robust software solutions – including the QUMAS Compliance Platform – that help global pharmaceutical, biotechnology, and medical device companies navigate complex regulatory landscapes and maintain operational excellence. Our platform streamlines document, quality, and incident management, ensuring adherence to regulations like FDA 21 CFR Part 11 and GxP guidelines.

QUMAS offers a comprehensive suite of services encompassing Electronic Document Management, Process Management (CAPA, Deviation, Change Control, Audit), and GMP Compliance Management, alongside specialized Regulatory Affairs solutions for submissions and data migration. We empower organizations to reduce reliance on multiple point solutions and simplify regulatory reporting, ultimately driving efficiency and minimizing risk.
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Contact Details

info@qumas.com

Cork, Ireland, No1, Cleve Busines Park

+1

Founded

1994

Company Type

Private Limited Company

Employees

50-100

Categories

Web Development
Developer Tools
Software

Keywords

#electronic document management

#process management (compliants

#capa

#deviation

#change control

#audit)

#gxp compliance management

#quality management

Awards

2026 OpenSee all

Products

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QUMAS Regulatory Affairs Solutions
Software

QUMAS Regulatory Affairs solutions provide submission management, including eCTD authoring templates, scanning and automated importing of paper documents, and document migration from legacy systems. It also offers collaborative review and full integration with leading publishing solutions.

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