Home

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.

In China, a food product is regulated under the State Administration for Market Regulation (SAMR), a combination of formerly China Food and Drug Administration (CFDA), Administration of Industry and Commerce (AIC), & Administration of Quality Supervision, Inspection, and Quarantine (AQSIQ). Freyr’s experts can assist you in any kind of food supplement Regulatory requirement in China such as food product classification, formulation/ingredient assessment, label & claims review, technical dossier compilation, submissions to the Health Authority, and many more.

Being the largest economy in Asia, it is no wonder that China is an attractive destination for cosmetic manufacturers. With a high rate of consumption and an ever-increasing consumer base, the Chinese cosmetic market experiences steady growth. As a leading global Regulatory partner, Freyr has extensive experience in providing cosmetic Regulatory services in China. Our team of Regulatory experts assists manufacturers to decode the China cosmetics registration process and ensure end-to-end compliance according to the China Cosmetic Supervision and Administration Regulation (CSAR).