The Anti-Telecommunication Network Fraud Law came into force on February 1 2022.
The Anti-Telecommunication Network Fraud Law consists of seven chapters and 50 articles, including general provisions, telecommunication governance, financial governance, internet governance, comprehensive measures, legal responsibilities and supplementary provisions. Efforts will be made to strengthen the prevention of legal system construction, strengthen the construction of cooperative working mechanism, increase the punishment of criminals, and promote the formation of anti-fraud, anti-fraud in the whole chain, anti-fraud in the whole industry and anti-fraud in the whole society.
The new law stipulates that the number of telephone cards handled shall not exceed the limit stipulated by the relevant state regulations. Telecom business operators have the right to strengthen verification or refuse to apply for cards if they find that there are abnormal card applications. Opening bank accounts and payment accounts shall not exceed the amount limited by relevant state regulations. Banking financial institutions and non-bank payment institutions have the right to strengthen verification of abnormal account opening or refuse to open an account.
New regulations on online drug sales: special drugs such as vaccines are not allowed to be sold online.
The General Administration of Market Supervision issued the Measures for the Supervision and Administration of Drug Online Sales, which will take effect on June 5438+February 1 day, 2022. The new regulations further standardize the online sales of drugs, especially prescription drugs, and online sales of drugs will truly usher in the era of strong supervision.
Article 42 of Chapter VI of the Measures stipulates the management of drug online sales, the performance of platform responsibilities, supervision and inspection measures and legal responsibilities. The main contents include: First, implement the main responsibility of pharmaceutical trading enterprises. Clarify the qualifications and requirements for pharmaceutical trading enterprises to engage in online sales of drugs, and clearly prohibit online sales of vaccines, blood products, narcotic drugs, psychotropic drugs, toxic drugs for medical use, radioactive drugs, pharmaceutical precursor chemicals and other drugs specially managed by the state according to law. The second is to compact the responsibility of the drug online sales platform. The third is to clarify the online sales management of prescription drugs. The fourth is to implement the "four strictest" requirements and strengthen the regulatory measures of regulatory authorities at all levels.
In addition, the "Measures" also clarified the corresponding legal responsibilities for online sales of illegal drugs according to law.
7 1 anticancer drugs and rare diseases can enjoy value-added tax concessions.
Recently, the Ministry of Finance and other four departments issued the third batch of anti-cancer drugs and rare disease drugs with VAT policy, including 5 1 anti-cancer drugs and raw materials, and 20 rare disease drugs and raw materials.
From 12 to 1 in 2022, for drugs in the catalogue, the value-added tax can be levied according to the simple method of reducing the domestic link by 3% and the import link by 3%.
The electronic certificate of drug export sales certificate was officially launched.
The State Administration of Pharmaceutical Products issued an announcement, starting from 1 2,2022,1,to enable electronic authentication for the export certificate of APIs and the export sales certificate of drugs.
Electronic proof and paper proof have the same effect. Combined with China's drug export practice and the latest WHO guidelines, a new drug export sales certificate template was introduced.
Quality management standard of cosmetics production: enterprises with serious defects should stop production.
The Inspection Points and Judgment Principles of Cosmetic Production Quality Management Standards issued by the State Administration of Medical Supplies will be implemented on June 5438+February 1 2022.
The Principles point out that the drug supervision and administration department should urge the enterprises judged as "defective in the production quality management system" to complete the rectification and submit the rectification report within the specified time, and organize on-site review when necessary. The pharmaceutical supervisory and administrative department shall, in accordance with the provisions of Article 54 of the Regulations on the Supervision and Administration of Cosmetics, take emergency control measures such as ordering to stop production and business to control product risks in a timely manner. The enterprise shall complete the rectification within the specified time and submit the rectification report to the drug supervision and administration department. The pharmaceutical supervisory and administrative department shall conduct on-site examination of the enterprise and confirm that the rectification meets the requirements before resuming production and operation.
New Regulation on the Supervision of Trademark Agency: Cleaning up the Agency that has not been engaged in business for a long time Recently, the General Administration of Market Supervision issued the Regulation on the Supervision and Administration of Trademark Agency, which will take effect on June 5438+February 1 day, 2022.
The "Regulations" further refine the regulations on institutional personnel, management system and code of conduct, and improve the overall service quality and development level of the industry from the source. Establish and improve the filing system of trademark agencies, clean up the agencies that do not carry out business for a long time and occupy industry resources by improving the filing procedures, and promote the formation of a benign development pattern of the industry. At the same time, in order to facilitate the filing of agencies, it is stipulated that trademark agencies shall not be required to provide information that can be obtained through government information sharing platforms.
The Regulations also require that the person in charge of filing a trademark agency must have certain conditions to prove that it has the ability to engage in trademark agency business, including the qualification certificate of trademark agent level examination, legal qualification certificate, intellectual property title, patent agent qualification certificate, etc.
New Edition of Safety Supervision Regulations for Railway Dangerous Goods Transportation: Strengthening Whole Chain Management
The Ministry of Transport issued the newly revised Regulations on Safety Supervision and Management of Railway Dangerous Goods Transportation, which will take effect on June 5438+February 1 day, 2022.
The revised Regulations further clarify the scope of dangerous goods: First, on the basis of the definition of dangerous goods in the current Regulations, it is clear that dangerous goods are identified in principle by the Railway Dangerous Goods List, and at the same time, it is further clear that those not included in the Railway Dangerous Goods List but identified as dangerous goods according to relevant laws, regulations and national standards need to be transported in accordance with the Regulations, which is not only convenient for practical operation, but also more comprehensive. Second, combined with the development of railway equipment technology, emergency prevention and control of epidemic situation and other dangerous goods transportation needs, the regulatory requirements of special circumstances under safety and technical conditions are clearly defined in supplementary provisions, so that the principle requirements are unified with special needs. The Regulations further strengthen the whole chain management of dangerous goods transportation.
New regulations on the management of Internet comment service: the system of trial before delivery should be established.
Recently, the National Internet Information Office issued the newly revised Regulations on the Administration of Internet Post Comment Services, which will take effect from June 5438+February 65438+May 2022.
The new regulations are clear, and if news information provides comments and comments, a preliminary examination system before publication should be established. Establish and improve information security management systems such as review management of post comments, real-time inspection, emergency response and report acceptance, timely discover and dispose of illegal and bad information, and report to the network information department. Equipped with audit editors suitable for the service scale, strengthen post review training and improve the professional quality of audit editors.
Legal basis: Measures for the Supervision and Administration of Drug Online Sales
Article 1 These Measures are formulated in accordance with the Drug Administration Law of People's Republic of China (PRC), the Cyber Security Law of the People's Republic of China, the Implementation Regulations of the Drug Administration Law of People's Republic of China (PRC) and other laws and regulations in order to regulate online drug sales, strengthen the supervision and management of online drug sales, and ensure the safety of public drug use.
Article 2 These Measures shall be observed in engaging in online drug sales activities, providing online drug trading services and their supervision and management within the territory of People's Republic of China (PRC).