China New GCP Effective Since May 1, 2022 2022-04-01 On March 31, 2022, NMPA officially released China new GCP (Medical Device Clinical Trial Quality Management Provisions, i.e.,… READ MORE > Impacts From China Standard Update On Medical Device Registration 2022-04-01 During the whole process of medical device lifecycle, the standards will be updated periodically. For example, GB 9706.1-2020… READ MORE > NMPA Updated Guidelines On Software, Cybersecurity And AI 2022-03-17 On March 7, 2022, NMPA published the updated Registration Review Guidelines on Medical Device Cybersecurity (Revision 2022), Registration… READ MORE > 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… READ MORE > 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… READ MORE > 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… READ MORE > 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… READ MORE > 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… READ MORE > 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… READ MORE > 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… READ MORE > New NMPA Review Guideline Of Animal Studies For Medical Device Registration 2021-11-27 On Sep 27, 2021, NMPA published a new Review Guideline of Animal Studies for Medical Device Registration: Part… READ MORE > New E-filing Catalogue For Medical Device Registration Effective Since Jan 1, 2022 2021-11-17 According to the Regulations on Supervision and Administration of Medical devices (Order 739), the Administrative Measures for Registration… READ MORE > Prev12345Next