Advisory and Consultancy Services

We will advise you on:

  • registration of persons and notification of medical devices;
  • the new Regulation of the European Parliament and of the Council (EU);
    • 2017/745 on medical devices,
    • 2017/746 on in vitro diagnostic medical devices.
  • classification of the medical device according to the degree of risk;
  • documentation of medical devices;
  • health technology assessment;
  • the reimbursement catalog;
  • the entry of the medical device into the foreign market.

Do you have any questions? Do not hesitate to contact us.