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Who can report? FAQ

Incident FAQ

"Medical devices adverse event" FAQ

complaints FAQ

What should be done immediately after the incident? FAQ

Are the requirements for reporting incidents and adverse events of medical devices included in clinical studies different from the general requirements? FAQ

SFDA urges home users to report accidents and problems of home use medical devices FAQ

"What is Field Safety Corrective Action?" FAQ

What is the procedure followed to appoint a manufacturer liaison officer or his authorized representative with SFDA? FAQ

When does SFDA set requirements for corrective actions for reported devices? FAQ