July

July 28, 2020

China PRER Due September 30, 2020: More Info to Help (II)

A Periodic Risk Evaluation Report (PRER) is required to submit to NMPA, depending on the initial NMPA registration time, according to Decree No. 1 Administrative Measures of Medical Device Adverse […]
July 28, 2020

NMPA: Continued Efforts on IP Protection, Fair Competition and Anti-Bribery

In March 2018, the transformation from CFDA to NMPA, which emerged into State Administration for Market Regulation (SAMR), was to make the linkage between pre-market approval and post-market surveillance, to […]
July 28, 2020

NMPA: Fourteen Guideline Issued in July

NMPA published 14 guidelines in July 2020. The guidelines cover indications of ophthalmic, orthopedic, gastroenterology and urology, anesthesia and immunology, etc. Full List of Guidelines General Technical review guideline on […]
July 28, 2020

China PRER Due September 30, 2020: More Info to Help (I)

A Periodic Risk Evaluation Report is required to submit to NMPA, depending on the initial NMPA registration time, according to Decree No. 1 Administrative Measures of Medical Device Adverse Event […]
July 23, 2020

China Medical Device UDI: First Batch Implementing October 1, 2020

NMPA “Rules for Unique Device Identification (UDI) System” Issued on August 27, 2019 mandates that the China UDI system for the first group of devices will take effect on October […]