NMPA Encourages High-quality Development Of Medical Device Industry 2022-02-23 In 2021, NMPA continues to encourage high-quality development of medical device industry through innovation pathway, priority pathway, real… NMPA New Regulatory Framework Summary In 2021 2022-02-16 In 2021, China NMPA established new regulatory framework for medical device registration. The below is a list of… China NMPA Newsletter – December 2021 2022-01-25 Inspirative Medical – A BradyKnows Company December 2021 China NMPA Newsletter Official Publication of BradyKnows 【Deadline】 2021 Annual… NMPA On Issuing Relevant Technical Guidelines In December 2021 2022-01-20 In order to strengthen the supervision and guidance of medical device product registration and further improve the quality… 【Deadline】 2021 Annual Quality System Self-Inspection Report To China NMPA 2022-01-18 Dear Medical Device Manufacturers, Here is a kind REMINDER to manufacturers operating Class III medical devices in China,… NMPA Collect Public Opinions On Termination Of Old GCP 2022-01-14 On Jan 12, 2022, NMPA issued a notice on its website to collect public opinions on termination of… New Batch Of China Medical Device Catalogue Modification 2022-01-05 On Dec 27, 2021, Center for Medical Device Standardization Administration of NMPA published a notice to collect public… NMPA Notice On Deadline Of Paying Review Fee For Registration 2022-01-05 On Dec 1, 2021, NMPA published a notice on the deadline of paying review fee for registration. After… China Continues To Enhance Post Market Surveillance On Medical Devices 2021-12-17 Since the implementation of Order 739 Regulations on Supervision and Administration of Medical Devices in June, 2021, China… China NMPA Newsletter – November 2021 2021-12-15 Inspirative Medical – A BradyKnows Company November 2021 China NMPA Newsletter Official Publication of BradyKnows New E-filing Catalogue… More Source Data Required For NMPA Clinical Trial Data Submission 2021-12-14 On Nov 25, 2021, NMPA published two guidelines on clinical data submission requirement for medical device and IVD… How To Handle China Registration During The Transition Period From Old NMPA Requirements To New Requirements 2021-12-08 The Administrative Measures for Registration and Filing of Medical Devices (Order No. 47) and the Administrative Measures for… « Prev...246...1112131415...18...Next »