Shulou(Shulou.com)11/24 Report--

CTOnews.com, November 30 (Xinhua)-- according to the Chinese government website, these new rules will affect your life and my life from December. Including the implementation of the Anti-Telecommunication Network Fraud Law of the people's Republic of China, the value-added tax concessions for these anti-cancer drugs and rare disease drugs, the implementation of the new regulations on Safety Supervision and Administration of Railway dangerous goods Transportation, and the implementation of the new regulations on online sale of drugs. the new regulations on trademark agency supervision will continue to strengthen the governance of the industry, and the key points and judging principles for quality management of cosmetic production will be implemented. The Electronic Certificate for the Export of EU Raw drugs and the Drug Export sales Certificate have been officially launched, and the Putonghua proficiency of primary and secondary school students will be divided into six levels.

Tuyuan Unsplash "Anti-Telecom Network Fraud Law of the people's Republic of China" implemented

The Law of the people's Republic of China on Anti-Telecommunication Network Fraud was adopted at the 36th meeting of the standing Committee of the 13th National people's Congress of the people's Republic of China on September 2, 2022, and will enter into force on December 1, 2022. The Law of the people's Republic of China against Telecom Network Fraud consists of seven chapters and 50 articles, including general principles, telecommunications governance, financial governance, Internet governance, comprehensive measures, legal liability, supplementary provisions, etc., based on various links, the whole chain to prevent and manage telecommunications network fraud, accurate force, to provide strong legal support for anti-telecom network fraud.

These anticancer drugs and rare disease drugs are entitled to VAT benefits.

Recently, the Ministry of Finance and other four departments released the third batch of anti-cancer drugs and rare disease drugs applicable to the value-added tax policy. These include 51 anti-cancer drug preparations and APIs, 20 rare disease preparations and APIs (click "read in detail" for the specific drug list). Starting from December 1, 2022, for the drugs on the list, the domestic link can choose to levy VAT by 3% simple method, and the import link can reduce the VAT by 3%.

The new edition of the regulations on Safety Supervision and Administration of Railway dangerous goods Transportation will be implemented

The Ministry of Transport has issued the newly revised regulations on Safety Supervision and Administration of Railway dangerous goods Transportation, which will enter into force as of December 1, 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 on the basis of the Railway dangerous goods name list, and at the same time, it is further made clear that for those who are not included in the Railway dangerous goods name list but are determined to be dangerous goods in accordance with relevant laws and regulations and national standards, they also need to be transported in accordance with the provisions. It is not only convenient for practical operation, but also comprehensively strengthen the safety supervision of the transportation of dangerous goods. Second, combined with the technical development of railway equipment, epidemic prevention and control emergency and other dangerous goods transport needs, in the supplementary provisions clear in line with the safety and technical conditions of the special circumstances of regulatory requirements, to achieve the unity of principle requirements and special needs. The revised "regulations" have also further strengthened the management of the whole chain of the transport of dangerous goods: first, it has increased the requirements for shippers in terms of protection measures, information notification, waybill filling, emergency contact, and so on, to strengthen the source management of the transport of dangerous goods. Second, it has increased the requirements for railway transport enterprises to sign safety agreements on the transport of dangerous goods with relevant units, and earnestly clarify the responsibilities of all parties to ensure transport safety. Third, according to the Anti-Terrorism Law, the requirements for positioning monitoring and information management of the means of transport of dangerous goods have been increased to ensure that the whole process of the transport of dangerous goods can be monitored and traceable. The fourth is to improve the relevant provisions of training, strengthen the requirements for transport units in the aspects of training outline, training courses and teaching materials, training files, and make it clear that employees should have relevant safety knowledge and other requirements. Fifth, increase the trial operation system, and require railway transport enterprises to organize relevant units to carry out trial operation for dangerous goods whose safe transport conditions are not yet clear, so as to effectively prevent transport risks and ensure transport safety. Sixth, according to the new "Law on Safety in production", the relevant requirements for the investigation and treatment of hidden dangers in the transportation of dangerous goods have been increased. Seventh, strengthen the emergency management of the transport of dangerous goods, increase the requirements of emergency plans and drills, emergency disposal, and so on.

New regulations on online sale of drugs implemented

The General Administration of Market Supervision and Administration has promulgated the measures for the Supervision and Administration of Drug Network sales, which shall enter into force as of December 1, 2022. There are 6 chapters and 42 articles in the measures, which provide for the management of drug network sales, the implementation of platform responsibilities, supervision and inspection measures, and legal responsibilities. The main contents include: first, the implementation of the principal responsibility of drug trading enterprises. Clarify the subject qualifications and requirements of drug trading enterprises engaged in drug network sales, and make it clear in accordance with the law that vaccines, blood products, narcotic drugs, psychotropic substances, toxic drugs for medical use, radioactive drugs, pharmaceutical precursor chemicals and other drugs under special control shall not be sold on the Internet. The second is to compact the responsibility of the drug network sales platform. The third is to clarify the network sales management of prescription drugs. Fourth, implement the "four most stringent" requirements and strengthen the supervision measures of regulatory departments at all levels. In addition, the "measures" also clearly defined the corresponding legal responsibilities for the illegal acts of online drug sales in accordance with the law.

New regulations on Trademark Agency Supervision will continue to strengthen Industry Governance

The General Administration of Market Supervision and Administration has promulgated the provisions on the Supervision and Administration of Trademark agents, which shall enter into force as of December 1, 2022. The "regulations" further refine the provisions on organizational personnel, management system, and code of conduct, so as to improve the overall service quality and development level of the industry from the source. We will establish and improve the filing system of trademark agencies, and clean up those agencies that have not carried out business for a long time and occupied the resources of the industry by improving the filing procedures, so as to promote the formation of a sound development pattern of the industry. At the same time, in order to facilitate the agency to handle the record, it is stipulated that the trademark agency shall not be required to provide repeatedly the information that can be obtained through the government information sharing platform.

Implementation of "Inspection points and judging principles of quality Management Standards for Cosmetic production"

The State Drug Administration has promulgated the key points and principles for the Inspection of Cosmetic production quality Management Standards, which will enter into force on December 1, 2022. The principles point out that for enterprises that are determined by inspection to be "defective in the production quality management system", the department responsible for drug supervision and administration shall urge them to complete rectification within the specified time and submit a rectification report, and may organize on-site review if necessary. For enterprises that are determined by inspection to be "seriously defective in the production quality management system", the department responsible for drug supervision and administration 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 the suspension of production and operation to control product risks in a timely manner. The enterprise shall complete the rectification within the prescribed time and submit a rectification report to the department responsible for drug supervision and administration. The department responsible for drug supervision and administration shall conduct an on-site review of the enterprise and confirm that the rectification and reform meet the requirements before resuming its production and operation.

The Electronic Certificate for the Export of EU Raw drugs and the Drug Export sales Certificate have been officially launched.

CTOnews.com was informed that the State Drug Administration has issued a notice to enable electronic certificates for the issuance of certificates for the export of EU APIs and drug export sales from December 1, 2022. Electronic certificates have the same effect as paper certificates. Combined with the practice of China's drug export and the latest guidelines related to World Health Organization (WHO), the new template of Drug Export sales Certificate is launched.

The Putonghua proficiency of primary and secondary school students will be divided into six levels.

The Ministry of Education and the National language work Committee issued the Putonghua proficiency Test Standard and Test outline for Primary and Middle School students (for trial implementation), which divides the Putonghua proficiency of primary and middle school students into six levels. the test content, scope, test paper composition and scoring standards are specified, which are suitable for the evaluation or monitoring of Putonghua proficiency of students in Grade 5 and above in compulsory education. The specification will be tried out on December 15, 2022.

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