Special software for medical devices, see “72 changes” of GSP compliance management of medical devices
On December 12, 2014, the State Food and Drug Administration issued the management quality specification for medical device business (GSP), which immediately became the red line of leading medical device enterprises’ business life and death. Once the line is touched, the consequences are very serious: minor rectification and fine, major cancellation and withdrawal of GSP certification certificate, resulting in the enterprise unable to operate. In the face of strict regulations, how to prevent and control the headache of GSP touch line risk? To seek the […]