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.