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Original title: The food and drug regulatory departments move the real guard "tongue tip safety
(China Medical News reporter Yu Haiping) In recent years, the national food and drug regulatory departments at all levels to strengthen food and drug safety supervision work, adhere to the most stringent standards, the most stringent supervision, the most severe punishment, the most serious accountability, focus on risk prevention and safety, focus on the field of food safety outstanding problems, crack down on illegal violations, from farmland to the table, from the laboratory to the hospital every line of defense to ensure the safety of the people.
To let children drink assured milk
In 2016, the State Food and Drug Administration investigated and prosecuted cases involving infant formula milk powder, especially in the case of "the production and sale of counterfeit infant formula milk powder" and "Shenzhen Yabei case", especially in the case of Jabe's (Shenzhen) dairy industry. The company's illegal and illegal activities, urged the local food and drug regulatory departments to make the confiscation of non-conforming products, fines and revocation of food production and operation license and other administrative penalties, and the company's legal representative and directly responsible for the competent personnel included in the food and drug violations of the enterprise "black list", take measures to prohibit the production and operation of food and related management for 5 years.
for the health of the next generation, the food and drug regulatory authorities strict infant formula milk powder supervision, the source of strict control, strict process control and a series of policy measures, so that children drink assured milk.
In order to ensure quality from the source, the food regulatory department requires enterprises to build their own or self-controlled milk source base, there is no self-built milk source base, there must be a stable supply and through regular audit and evaluation of raw material suppliers to implement the raw materials into the factory batch inspection and inspection, from the source to ensure quality and safety. The implementation process is strictly controlled, through the formulation of licensing and registration conditions to raise the entry threshold for enterprises, urge enterprises to implement good production practices and hazard analysis and key control point system, strict production environment, production equipment operating status and production process management. The factory products to implement the whole project, batch-by-batch inspection. Enterprises are required to establish food safety traceability system and product tracking evaluation norms.
china currently has infant formula milk powder production enterprises 108, and now some enterprises have reached the world's advanced production conditions, scale. In 2016, the General Administration carried out 22 inspections of the production system of infant formula milk powder production enterprises, sampling 2532 batches of infant formula milk powder, with a pass rate of 98.7%.
the internet to order convenient and safe
days ago, Beijing Daxing District Food and Drug Administration on the "hungry" platform of the three undocumented operating shops to be investigated and punished in accordance with the law.
Ningbo City on the United States group takeaway, Baidu takeaway, hungry and other three companies have been ordered to correct and fine 120,000 yuan of administrative penalties, because it did not in accordance with the law to access the network of food operators real-name registration and examination permits.
the era of sharing economy, network ordering has brought convenience to public life, but also increased the difficulty of supervision. The safety of online ordering has become a hot issue of public and media concern.
In July 2016, the State Food and Drug Administration stepped up the supervision of food safety on the Internet, promulgated the Measures for the Investigation and Punishment of Food Safety Violations on the Internet, and recently published the Measures for the Supervision and Administration of Internet Food Service (Draft for Comments), focusing on whether the third-party network ordering platform implements the responsibility for food safety management, whether food service operators operate online with valid food business licenses and truthfully disclose food licensing information, and so on.
all over the food and drug regulatory departments to use joint law enforcement, investigation and prosecution and other ways to carry out network food "net" action, in 2016, only in Beijing, Shanghai, Guangzhou, three places have accumulated off-line problems of catering operators more than 90,000 households.
Drug review speed up the use of drugs more timely
the first drug market licensing system pilot varieties "Gifeitini" was approved; Since August 2015, drug review and approval has entered the "reform time", and a series of reform measures have been introduced, such as the reform of chemical drug registration classification, the system of drug listing license holders, the consistent evaluation of generic drugs, and the priority review and approval, and the results of the reform have gradually emerged.
2016, the State Administration of Food and Drug Administration adhered to the principle of review in accordance with regulations and scientific norms, conducted collective deliberations on all drugs to be listed, and approved a total of 206 applications for registration of pharmaceutical production (listing). Priority review was carried out on 193 innovative drugs with obvious clinical value, clinically urgent needs, patent expired drugs and domestic first generic drugs, and a new generation of fluoroquinoquinosterone-free drugs was given 1.1 class 1.1 new drug neonicotic capsules, the world's first effective prescription for the treatment of influenza A(H1N1) Fang, double-priced hpedillomavirus adsorption vaccine (HPV vaccine), poliovirus-reducing live vaccine sugar pills (human double body cells), 13-price pneumococcal polysaccharide combination vaccine and other innovative drugs were approved, further shorten the market cycle of new drugs, so that the reform dividend really benefits the general public.