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Imported medical devices should be registered or filed in accordance with relevant regulations. The customs shall inspect imported medical devices in accordance with the law; if they fail the inspection, they shall not be imported.
The registration methods of imported food overseas production enterprises include registration recommended by the competent authorities of the country (region) where the enterprise is located and registration application. According to Article 16 of the "Regulations on the Regulations on the Registration of Foreign Manufacturers of the People's Republic of China", after the enterprise applied for registration, the registration period of overseas manufacturers of imported food is valid for 5 years.
The validity period of the medical device registration certificate is stipulated according to the classification of medical device products. During this validity period, medical device companies can produce and sell medical devices in accordance with the provisions of the registration certificate.
With rapid development of cosmetics industry and continuous improvement of consumer awareness, cosmetic ingredients or active raw materials are gradually becoming known and paid attention to by consumers.
Medical device registrants, filers, and entrusted manufacturing enterprises shall regularly conduct self-examinations on the operation of the quality management system and submit self-inspection reports in accordance with the regulations of the State Council’s drug regulatory department.
According to the provisions of new regulations, when declaring cosmetics to NMPA, all ingredients except water must have "raw material quality and safety information documents" before they can be declared, and the applicant must upload the document to the database.
