Post-market Periodic Risk Evaluation Report Mandatory For License Holder In China 2022-06-29 As per Measures for the Monitoring and Re-evaluation of Medical Device Adverse Events, NMPA has regulatory requirements for… READ MORE > NMPA Enhances Cross-reginal MAH Surveillance 2022-05-30 The implementation of medical device MAH in China is aiming at promoting the reform of medical device review… READ MORE > Interpretation Of Relevant Regulatory Documents And Response Strategies On China National Medical Device Quality Sampling And Inspection Work In 2022 2022-03-23 In recent years, with the national policy and the continuous adjustment and optimization of the industrial structure around… READ MORE > NMPA Strengthening The Supervision And Management Of Medical Device Registration 2022-02-27 In 2021, NMPA continues to strengthen the supervision and management of medical device registration. Class I filing surveillance… READ MORE > NMPA AE And Recall Report In October 2021 2021-12-02 In October, 2021, NMPA published the AE and recall list reported by overseas manufacturers. Since China NMPA enhances… READ MORE > NMPA AE And Recall Report In September 2021 2021-12-02 In September, 2021, NMPA published the AE and recall list reported by overseas manufacturers. Since China NMPA enhances… READ MORE > NMPA AE And Recall Report In August 2021 2021-09-02 In August, NMPA has released 28 medical device recalls, 14 of which are imported products. The table below… READ MORE > NMPA AE And Recall Report In July 2021 2021-08-02 In July, NMPA has released 17 recalls regarding the imported medical devices in China. The table below is… READ MORE > NMPA AE And Recall Report In June 2021 2021-07-07 In June, NMPA has released 14 recalls regarding the imported medical devices in China. The table below is… READ MORE > Be Careful! What Kind Of Mistakes Lead To Recalls In China? 2021-06-04 From May 21 to 26, 2021, seven overseas manufacturers voluntarily recalled different medical devices.Most of the recalls involved… READ MORE > Prev12