Scan the electronic supervision code to know the authenticity of the drug

Scan the electronic supervision code on the drug packaging, and the drug information can be traced back to the 23rd. The Yantai Food and Drug Administration held a press conference to notify the development and completion of the GSP certification work of drug dealers and the electronic supervision of drugs. All companies are by the end of October Full-species electronic supervision will be implemented, and the whole process of traceable electronic supervision of drugs will be realized before the end of the year. Once the electronic supervision code is scanned, all drug information can be checked. According to the requirements of the National Drug Safety 'Twelfth Five-Year Plan'The electronic supervision code is the identity card of the drug.' According to Liu Wenbin, deputy director of the Yantai Food and Drug Administration, all drugs must obtain a drug approval number, and the implementation of electronic supervision code management is equivalent to having a second drug.' ID card'. After the implementation of electronic drug supervision, it will rely on the Internet and computer systems to establish a national network platform for the dynamic supervision of drug production, circulation, and use through the entire process of verification and write-off, and provide technology for drug anti-counterfeiting, anti-counterfeiting, traceability, and recall. support. At that time, the drug regulatory authority will use computer management systems, law enforcement equipment and other tools to monitor the entire process of drug delivery, circulation, storage, delivery to medical institutions, and sales to consumers, and through terminal mobile law enforcement, real-time inquiries and grasps of the true nature of drugs listed on the Internet The basic information of fake and varieties and the situation of production, sales, inventory, etc. At the same time, consumers can check the authenticity of medicines on the terminal through mobile phones, fixed telephones, and Internet access. On the 23rd, the reporter saw the electronic supervision code printed on the packaging on an oral liquid at the Lijian Pharmaceutical chain store in the coastal district. After logging in to the China Drug Electronic Supervision Network, the generic name of the drug is displayed as Pudilan Anti-inflammatory Oral Liquid, and the dosage form, manufacturer, production date, product batch number, expiration date, and approval number are all available. The circulation information shows that the drug has flowed to Shandong Lijian Pharmaceutical City Chain Co., Ltd. Liu Wenbin introduced that at present, 3457 pharmaceutical retail companies have introduced electronic supervision networks, 3147 confirmed, 2677 companies have held digital certificates, the network access rate is 76.95%, and more than 700 companies upload data. All companies will implement electronic supervision of all varieties before the end of the year. . GSP certification for pharmaceutical companies 　 The news conference held by Yantai Food and Drug Administration will also introduce the GSP certification status before the end of October. As of September, there were 47 wholesale companies in the city and 46 certified; 65 retail chain headquarters, and 58 on-site inspections; 3,432 retail stores and single pharmacies, and 3032 on-site inspections; according to the work plan, the city’s drug operating companies The certification work will be completed before the end of October. The so-called GSP is the 'Pharmaceutical Business Quality Management RegulationsTo ensure the safety of the public’s medication. The newly revised GSP has comprehensively upgraded the software and hardware standards and requirements of enterprise operations, and raised the barriers to market access. A series of new regulations have been added to the current weak links in drug circulation, such as irregular drug business behavior, unclear purchase and sales channels, chaotic bill management, entrusted third-party logistics, and cold chain management. Controlling the number of retail pharmacies and encouraging corporate mergers and reorganizationsAccording to reports, in terms of advancing drug business supervision, the Food and Drug Administration has brought unannounced inspections into the normal, without greeting, went straight to the company, and withdrew the GSP certificate for serious violations of the ``Pharmaceutical Business Quality Management Regulations''. It also announced the cancellation, resolutely investigate and deal with enterprises that purchase and sell counterfeit and inferior drugs in accordance with the law, and revoke the 'Drug Business License' to be publicly announced. The Yantai Food and Drug Administration will supervise the administrative licensing situation of the city, and announce the cancellation of the 'Pharmaceutical Business License' that violates the regulations; the 'Pharmaceutical Business License' will not be renewed for those that have not passed the GSP certification. Resolutely cancel the expired licenses, and control the number of retail pharmacies opened in accordance with Article 14 of the Drug Administration Law, 'follow the principles of reasonable layout and convenient drug purchase by the masses. In terms of drug electronic supervision, increase the efforts of retail enterprises to access the Internet. Enterprises are required to obtain a digital certificate when applying for certification, and when receiving a certification certificate, they must verify and write off and upload data, and urge enterprises to verify and write off in a timely manner. Companies will be urged to do a good job in maintaining corporate information on the drug electronic supervision platform, and companies will be urged to scan, verify and write off the code when they see the code, upload data in a timely manner, and achieve the goal of the entire process of traceable drug electronic supervision before the end of the year.