Delcon quality & environment policy
Pursuing its mission to provide blood bag manufacturers with state of the art devices to be used with the consumable materials and transfusion and plasma collection centers with tailored solutions that increases the overall efficiency and efficacy of their operations, Delcon considers the quality of its products and services and the protection of the environment, key elements of its business strategy.
Quality forms an integral part of Delcon’s corporate business principles, which have always guided our actions in order to provide innovative and competitive products and services that are safe and compliant, in the respect of nature. They are a key to being recognized and identified on the world scenario as a manufacturer of medical devices that improve the quality of life and contribute to public health.
Delcon ensures compliance of its products with the European Medical Devices Regulation (MDR) 745/2017, the European In Vitro Diagnostic Medical Devices Regulation (IVDR) 746/2017 and compliance with the Canadian Medical Device Regulation (SOR/98-282). Furthermore Delcon’s Quality Management System meets the requirements of EU ISO 13485:2016 and of US Quality System Regulation (FDA 21 CFR Part 820, 803, 807, 11).
At Delcon, we are all involved in reaching our objectives. Every one of us has the power to influence the constant improvement that we wish to achieve through our actions and involvement. The trust that our customers place in the quality of our products and our capabilities is an asset that we wish to support, so we share our policy within the company and outside with our stakeholders, considering them an integral part of and partners in our commitment to the objective of excellence.