Today we have received the certificates guaranteeing that NeuroSoft Company meets the requirements of Council Directive 93/42/EEC of 14 June 1993 concerning medical devices and apply the system of quality assurance for our system manufacture stages and product test. After having received these certificates we have a right of drawing CE mark on the following systems:

This is a significant event in our company's life. Now our production can be sold on international markets where CE certificate is required. This is the successive step of the quality system formation. The next step will be the enlargement of the number of digital systems certified according to European requirements.

This page last updated on November 11, 2004.