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Based on our practical experience and advanced language skills in the field of expertise, HMK’s translation service in medical device covers all stages of medical device documentation, from product research, product planning, product development, registration application to all post-market services.
New food ingredients need to be reviewed and approved by the health administrative department of the State Council (i.e., the National Health Commission) before they can be used in food production in China. During the review process, the National Food Safety Risk Assessment Center will conduct a technical review.
The registration and certification of medical products is the first threshold for companies to export into various countries. Registration certificates of medical devices are a key factor for companies to win customers in competition.
According to the “Food Safety Law of the People's Republic of China”, new food additive varieties must be reviewed and approved by the health administrative department of the State Council before they can be used in food.
The veterinary diagnostic products (including reagents such as antigens and antibodies, nucleic acids, proteins, and tumor markers) industry is an important part of the veterinary drug industry. Veterinary diagnostic products are important tools for diagnosing and monitoring diseases.
According to the "Administrative Licensing Regulations on New Varieties of Food-Related Products", new varieties of food additives refer to new varieties of food-related products. It refers to food packaging materials, containers, detergents, disinfectants, and tools, new materials, new raw materials or new additives for equipment used in food production and operation.
