- 1- Вы задавались вопросами:
- 21. «Можно ли, внести изменения в РУ 2006 г.?»
- 22. «Требуется ли, переоформление РУ при смене организационной формы?»
- 23. «Как присвоить вид медицинского изделия в соответствии с Приказом № 4н от 06.06.2012 г.?
The Russian legislation specifies control of all processes in the area of utilization of medical products in the territory of the Russian Federation.
The main task of the supervisory authority is to take measures, which help find and eliminate all possible violations by entities employed in the field of manufacturing and sales of medical products.
Activity of organisations in the area of utilization of medical products is controlled by the supervisory authority by means of scheduled and off-schedule inspections.
Activity of manufacturers (representatives) of medical products should strictly comply with the statutory regulations. To prevent violations, all manufacturers of medical products should know the processes of the governmental control.
Also, it's important to be familiarized with the procedure of inspections of legal entities and individual entrepreneurs employed in the area of utilization of medical products.
You can also obtain the additional legal information , which will help you familiarize yourself with all aspects of the Russian legislation in this area in detail.
Knowledge of all the legal aspects of utilization of medical products is the basic premise for successful entrepreneurship of all manufacturers (representatives) of medical products.
Ignorance of the law is no excuse!