freyrsolutionschina

[freyrsolutionschina]

China is one of the fastest-growing markets for Medical Devices, where the demand for devices is majorly met through imports. NMPA (National Medical Products Administration) ,formerly known as CFDA and the Centre for Medical Device Evaluation (CMDE) are responsible for the review of the Medical Device import registration applications of all the three (03) classes of devices (Class I, II & III). As per NMPA regulations, an NMPA legal agent must be appointed to serve as a representative of overseas pharmaceutical and medical device companies applying for China Medical Device Registration.

#NMPA #CMDE #NMPA regulations

[freyrsolutionschina]

#Regulatory Services in China #China NMPA Registration #Regulatory Affairs China #NMPA Registration #NMPA Regulations #Regulatory Approval Process in China