Quality Policy

October 2023
Pragmatech was founded in 2021 with the goal of developing pragmatic AI solutions to address challenges beyond health and life sciences. For this purpose, our company:

Develop solutions based on artificial intelligence in the field of infectious diseases and microbiology.

Through these solutions, the objective is to contribute to improving the diagnosis and prognosis of these diseases as well as the quality of life of the people who suffer from them.

Develop products aimed at helping the prescription of antibiotics and optimizing their use from a holistic and One Health perspective.

The optimization of the use of antibiotics will contribute to the fight against resistance to them, one of the main threats to public health worldwide.

The fundamental pillars on which Pragmatech’s QUALITY management is based are:

The concept of modular platform contributed to our solutions, from which different sanitary products with multiple functionalities are developed.

The medical devices supplied to our customers are safe, robust, reliable and meet the requirements established in the applicable legislation and harmonized standards.

The closeness to our interest groups and the exhaustive analysis of their needs and expectations, to develop innovative sanitary products in different fields.

The Pragmatech team has extensive experience in the field of application of its products, both in terms of R&D and healthcare.

The achievement of excellent working conditions and environment that allow high satisfaction of the multidisciplinary and international work team that forms Pragmatech.

Improving the quality of healthcare products and services provided by analyzing data and identifying areas for improvement, collaborating jointly with the stakeholders involved.

PRAGMATECH pursues the continuous improvement of strategic, operational and support processes, through an effective implementation of its Quality Management System, in accordance with the requirements established in the ISO 13485 standard (Healthcare products, Quality management systems, requirements for regulatory purposes) and Regulation (EU) 2017/745 of the European Parliament and of the Council, of April 5, 2017, on medical devices, the scope of which is defined as:

Design, development, marketing, installation and maintenance of health software products.