Guideline for Quality Management System Inspection on Medical Device Registration
On March 17, 2020, NMPA released a Guidelines for Quality Management System Inspection on Medical Device Registration in order to further strengthen the its surveillance on medical device registration. Bradynuoen suggest manufactures to follow the new QMS requirements to do relevant manufacturing and registration. Since China NMPA enhances the registration and product surveillance, Bradynuoen can help manufacturers to evaluate the gap between your products and new guidelines.
