A large number of the above-mentioned medical devices have been detected

The frequent occurrence of major and important cases shocked the industry, and also caused a lot of confusion to operating companies and medical institutions: how to prevent such problems? In this revision, a new provision has been specifically added that operating enterprises and medical institutions can be exempted from fines. Wait.　　

On May 4, 2016, the Legislative Affairs Office of the State Council publicly solicited opinions on the 'Draft for Review'. This is in line with the 'Related Policies on Encouraging Drug and Medical Device Innovation and Reforming Clinical Trial Management' (Draft for Solicitation of Comments)' The new regulations are consistent. 　　

For the addition of these contents, the National Health and Family Planning Commission’s 'Draft for Review' 'The drafting instructions have clearly stated that medical institutions generally have the urge to expand the size of beds and large-scale medical equipment. This shows that in the past year, the industry's regulatory situation has changed again.

And report to the State Council for review.Respiratory Protective Mask Especially since the regulations on the management and use of medical devices have been promulgated, the supervision of the drug regulatory department has extended from production to operation and use.

A large number of the above-mentioned medical devices have been detected, and a large number of operating companies and users have also been punished by administrative punishments. There are many high fines and major cases.