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 > New China GCP To Be Issued Soon 2021-11-10 As a member of IMDRF (International Medical Device Regulators Forum), China is actively leading and participating in the… READ MORE > New Requirements For Medical Device And IVD Registration Application Dossiers 2021-11-03 More and more new guidelines are published according to the Regulations on Supervision and Administration of Medical devices… READ MORE > Official NMPA Regulation Released: Self-Testing For Medical Device Registration In China 2021-10-27 Fundamental of Type Testing Type testing, also known as medical device registration testing, is a mandatory requirement by… READ MORE > Prev1234Next