Disinfection products is an important weapon to protect public health, but if the production is unqualified, it will lead to serious consequences. Therefore, in order to ensure the quality and safety of disinfection products, the state implements a filing system for disinfection products. Disinfection products filing means that disinfection products production enterprises can produce and sell products only after submitting their applications for product filing to National Medical Products Administration. Disinfection products's filing requirements include but are not limited to the following: product standards meet national regulations; The production process conforms to the national standards; Technical documents such as drug inspection reports meet the requirements of the state; The product samples meet the requirements and the storage conditions meet the requirements. At the same time, the drug supervision department will also review the production management and technical level of the production enterprises to ensure that the production enterprises have the ability and qualification to produce such products. It is worth mentioning that disinfection products filing is different from drug listing permit. Disinfection products needs continuous quality supervision and monitoring after listing to ensure that products meet the standards and protect public health.
What should I do if I find that my disinfection products has not been filed? Consumers can report or complain to the local drug supervision department. Production enterprises that produce and sell without filing will face administrative penalties such as fines, suspension of production and rectification, and may be listed as "bad credit records".
Filing in disinfection products is an important measure to protect consumers' safety and health. Production enterprises should carry out production in strict accordance with the requirements of national standards, and drug supervision departments should also strengthen supervision over production enterprises to ensure that the disinfection products produced meets the requirements and protect public health.
Legal basis:
Article 13 of the Regulations on the Supervision and Administration of Medical Devices shall, in accordance with the relevant national technical requirements and standards, formulate, implement and supervise production control and inspection standards to ensure the safety, effectiveness and stability of medical devices.