Quality control


The Management of IMED Ltd. in proper time got wise to the fact, that the production of quality products, the marketability and the market extensibility (especially considering the European Union) crucially requires the firm to operate and maintain Quality Management System that meets the requirements of the ISO 13485:2016 standard and established according to the relating EU Medical directives as certified by the EMKI.

The precondition for our exportation activity into the American continent was the fulfilment of the FDA regulatory pathway, that was succeeded in.

As our quality policy states:

„…our goal is the development and production of modern medical devices that effectively support the physicians and doctors, hereby raising the quality of health care”