Digitize your Quality Management System – Webinar Replay Available HERE

In regards to

GxpManager

Software publisher since 2003 GxpManager offers a No Code Low Code solution in SaaS architecture (i.e. in the Cloud) for companies who need to process critical data such as in the pharmaceutical sector (…).

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Develop without programming

The goal is to develop applications, without programming, that meet all the requirements around the critical data digitization in the company: electronic signature, audit trail (i.e. the traceability of captured data in the solution), access management, data uniqueness, workflow, data and documents secure storage, infrastructure and applications validation. Critical data can be inspected at any time by customers, regulatory bodies or normative authorities, such as the ANSM in France, the FDA in the USA for the health sector in order to ensure the data uniqueness and integrity.

GxpManager innovates with its No Code Low Code solution

Jérôme Tomaselli, president of GxpManager, explains the challenges of digital transformation and the advantages of using the GxpManager platform during the program LE GRAND ENTRETIEN presented by Michel Denisot on B SMART TV channel.

GxpManager In Numbers

+ than 20 apps

Ready to use or from an application model.

+ 1000 projects

made with the GxpManager platform

+ 5000 licenses

sold since 2003

+ 25 years of expertise

Life Sciences, regulated sectors, medical devices, services, industries…

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Last news

News
The Expert in Digitizing Critical Data

A medical device's risk analysis is an essential step in ensuring that it complies with current regulations and is safe for users. In this field, digitizing critical data helps ensure data compliance, safety, and reliability.

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News
GxpManager: Recognized Vendor in Gartner’s Hype Cycle for Quality by Design

Quality by Design (QbD) has emerged as a critical framework in product development and quality assurance. Its systematic approach, rooted in science and quality risk management, has garnered significant industry attention.

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News
Digitizing a medical device’s risk analysis to guarantee compliance

A medical device's risk analysis is an essential step in ensuring that it complies with current regulations and is safe for users. In this field, digitizing critical data helps ensure data compliance, safety, and reliability.

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Use cases
Artworks: Management of packaging items and promotions

Management and validation of Artwork in-house up to the publication for the printer (subcontractor) for an international pharmaceutical company, with a 20% time-saving in validation.

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News
Vivatech 2023 – Innovation and digitization

From June 14th to 17th, the Viva Technology trade show was held at Paris Expo Porte de Versailles, and our colleagues were on hand to present the future of critical data digitization.

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News
The 7 Principles of Quality Management

GxpManager offers medical device manufacturers a digitization platform based on a Low Code No Code concept to meet regulatory requirements for the integrity and traceability of critical data…

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