NMPA Facilitates The Usage Of Medical Device Master Files 2023-01-31 The NMPA issued a notice on further clarifying matters related to the registration and use of the master… READ MORE > NMPA Collects Public Comments On Guidelines For Registration Review Of Implantable Medical Device Battery 2023-01-05 In order to standardize the requirements for technical review and guide the registration and application of enterprises, CMDE… READ MORE > NMPA Medical Device Classification Catalogue Updating 2022-11-22 According to the Working Procedure for Dynamic Adjustment of the Medical Device Classification Catalogue and related requirements, the … READ MORE > The Third Batch Of Medical Device Product Classification Identification In 2022 2022-11-22 Center for Medical Device Standardization Administration, a branch of NMPA, issued a summary of the third batch of… READ MORE > NMPA Notice On Adjustment Of Technical Consultation About Medical Devices Registration Before Application Acceptance 2022-11-22 In order to comprehensively promote the development of China’s medical device industry and give full play to the… READ MORE > Guidelines On The Registration Of Registered Class II Medical Devices Moving Into Guangdong Province 2022-09-17 In order to continuously optimize the business environment and promote the high-quality development of the medical device industry… READ MORE > NMPA Notice On Matters Related To The Filing Of Class I Medical Devices 2022-08-19 In order to do a good job in the filing of Class I medical devices, the NMPA issued… READ MORE > NMPA Gives Full Support To China Real World Data Application Pilot Projects 2022-04-27 On April 22, 2022, NMPA published a Communication Procedure for Medical Device Real World Data Application Projects in… READ MORE > Key Updates In New Version Of China GMP Compared With Old Version 2022-04-12 On March 22, 2022, NMPA published the updated version of China GMP (Good Manufacturing Practice) and GSP (Good… READ MORE > 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 > Prev1234Next