When do I need GMP certificate for medical device declaration?

The regulations require 65438+ 10/0/this year, and the final limit of some provinces and cities is July 1, but many provinces and cities have begun to implement new GMP requirements for medical devices.

At present, the country only implements GMP for sterilized and implanted products, and other product management norms are being formulated.

If it is an enterprise that needs GMP, it must be highly concerned. The new specification involves a lot of infrastructure rectification.

Aozida Medical Device Consulting Organization (Guangzhou, Beijing, Shanghai, Suzhou, Shenzhen, USA)