Legal advice on compliance of medical devices with mandatory labeling requirements

Advising leading Swiss producer of pharmaceuticals and medical devices on general legal framework and specific labeling requirements under Ukrainian law applicable to the imported medical devices on the outer packing and instructions for use (e.g. minimum content, layout and design of packing, use of special symbols, language requirements, etc.) as well as consulting on some particulars of mandatory certification and state registration of medical devices with Ukrainian competent authorities.