Quality Policy

The management of IONCLINICS DEIONIC, S.L. proclaims the following declaration of “Quality Policy”, and  undertakes to disseminate it and make it understood throughout the company and, where appropriate, to its customers and suppliers , as well as to review it and keep it continuously adequate

The Management of IONCLINICS DEIONIC, S.L. wants to maintain its commitment to promote quality and to unite all our efforts in this general objective, the “Quality of our Management System of our activity as a manufacturer and importer of medical devices”. It is our aim to work at the level set by the International Standard, UNE-EN 13485:2018 (EN ISO 13485:2016+A11:2021) and Directive 93/42/EEC / Regulation (EU) 2017/745), and to ensure that our activities as manufacturers importers and distributors of medical devices comply with the legal requirements, regulations and specifications, market and customer needs that affect them in each case. (P1)

The Management assumes the commitments to provide its customers only with services that satisfy them, to establish capable processes and to comply with a programme of continuous improvement of the effectiveness of the Quality Management System, Manufacture, Import and Distribution of Medical Devices.

Consistent with the decision and will expressed, the Management is committed to providing the human and material resources, infrastructure, training and training of personnel and the right working environment to achieve its objectives, in the conviction that the cost involved is nothing other than a profitable investment.

Another important objective for the Organisation is that all its personnel have a global vision of the project they are working on, so that they feel part of it and increase their motivation. Quality is an objective and a responsibility of all the personnel integrated in the Organisation. Each employee is responsible for the quality of their own work.

Convinced that Quality will help us to achieve a system of continuous improvement, specific, quantifiable objectives will be established and reviewed annually by the Management, with defined responsibilities and deadlines for execution, which will help us to objectively evaluate the improvement achieved.

The Quality, Manufacturing Importation and distribution of Medical Devices Policy will be made known to all staff through internal dissemination of the same

I ask the staff of IONCLINICS DEIONIC, S.L. to assume and abide by the provisions of the Quality Management Manual and I delegate the general responsibility for supervising the effectiveness, implementation and maintenance of the Management System to the Quality Manager and Technical Manager as representative of the Management.