Heavy! These enterprises suspend production and are ordered to suspend production! ! !

December is approaching, and a batch of new regulations that are closely related to life will be implemented soon, involving these aspects! !

From December 1st, these anti-cancer drugs and rare disease drugs can enjoy preferential value-added tax

Recently, the Ministry of Finance and other four departments released the third batch of anti-cancer drugs and rare disease drug lists applicable to the VAT policy, including 51 anti-cancer drug preparations and raw materials, 20 rare disease drug preparations and raw materials (specific drug list Click "Read More" to view). From December 1, 2022, for the drugs in the list, the domestic link can choose to calculate and levy value-added tax according to the simple method of 3%, and the imported link can be levied at a reduced value-added tax of 3%.

The new version of the "Regulations on the Safety Supervision and Administration of Railway Transport of Dangerous Goods" will come into effect on December 1

The Ministry of Transport issued the newly revised "Regulations on the Safety Supervision and Administration of Railway Transport of Dangerous Goods", which will come into force on December 1, 2022.

The revised "Regulations" further clarifies the scope of dangerous goods:

First, on the basis of the definition of dangerous goods in the current "Regulations", it is clarified that dangerous goods should be identified in principle based on the "List of Dangerous Goods on Railways" Dangerous goods determined according to relevant regulations and national standards also need to be transported in accordance with the "Regulations", which is not only convenient for practical operation, but also comprehensively strengthens the safety supervision of the transportation of dangerous goods.

The second is to combine the development of railway equipment technology, epidemic prevention and control emergency and other dangerous goods transportation needs, in the supplementary regulations, the regulatory requirements for special situations that meet the safety and technical conditions are clarified, so as to achieve the unity of principle requirements and special needs. The revised "Regulations" also further strengthened the management of the entire chain of dangerous goods transportation: First, increased the requirements for shippers in terms of protection measures for dangerous goods, information notification, waybill filling, emergency contact, etc., and strengthened the source management of dangerous goods transportation.The second is to increase the requirement for railway transport enterprises to sign dangerous goods transport safety agreements with relevant units, and effectively clarify the responsibilities of all parties to ensure transport safety.

Third, according to the "Anti-Terrorism Law", the requirements for location monitoring and information management of dangerous goods transportation vehicles have been added, so that the whole process of dangerous goods transportation can be monitored and traced.

The fourth is to improve the relevant regulations on training, strengthen the requirements for transport units in terms of training outlines, training courses, teaching materials, and training files, and at the same time clarify the requirements that employees should have relevant safety knowledge.

The fifth is to increase the trial transportation system. For dangerous goods such as new product names and new packaging that have not yet specified safe transportation conditions, railway transportation companies are required to organize relevant units to conduct trial transportation to effectively prevent transportation risks and ensure transportation safety.

Sixth, according to the new "Safe Production Law", relevant requirements for the investigation and management of hidden dangers in the transportation of dangerous goods have been added.

The seventh is to strengthen the emergency management of the transportation of dangerous goods, and increase the requirements for emergency plans, drills, and emergency disposal.

New regulations on drug online sales will come into effect on December 1

The State Administration for Market Regulation issued the "Measures for the Supervision and Administration of Drug Online Sales", which will come into force on December 1, 2022.

The "Measures" has 6 chapters and 42 articles. It stipulates the management of drug online sales, the performance of platform responsibilities, supervision and inspection measures, and legal responsibilities. The main contents include:

The first is to implement the main responsibility of drug distribution enterprises. Clarify the qualifications and requirements of pharmaceutical business entities engaged in online sales of pharmaceuticals, and clarify in accordance with the law vaccines, blood products, narcotic drugs, psychotropic drugs, toxic drugs for medical use, radioactive drugs, pharmaceutical precursor chemicals, and other drugs that are subject to special management in the country Not for sale online.

The second is to consolidate the responsibilities of the drug network sales platform.

The third is to clarify the online sales management of prescription drugs. The fourth is to implement the "four most stringent" requirements and strengthen the supervision measures of supervision departments at all levels. In addition, the "Measures" also clarified the corresponding legal responsibilities for illegal drug online sales in accordance with the law.

"Anti-Telecommunications Network Fraud Law of the People's Republic of China" came into effect on December 1

The Anti-Telecommunication Network Fraud Law of the People's Republic of China was passed at the 36th meeting of the Standing Committee of the Thirteenth National People's Congress of the People's Republic of China on September 2, 2022, and will come into force on December 1, 2022. The "Anti-Telecommunications Network Fraud Law of the People's Republic of China" has seven chapters and 50 articles, including general principles, telecommunication governance, financial governance, Internet governance, comprehensive measures, legal responsibilities, supplementary provisions, etc., based on each link and the whole chain to prevent and control telecom network fraud, and accurately Make efforts to provide strong legal support for the anti-telecommunication network fraud work.

New regulations on trademark agency supervision will continue to strengthen industry governance

The State Administration for Market Regulation issued the "Regulations on the Supervision and Administration of Trademark Agents", which will come into force on December 1, 2022.

The "Regulations" further refine the regulations on institutional personnel, management systems, codes of conduct, etc., and improve the overall service quality and development level of the industry from the source. Establish and improve the filing system for trademark agencies. By improving the filing procedures, agencies that have not conducted business for a long time and occupy industry resources will be cleaned up to promote the formation of a healthy development pattern for the industry. At the same time, in order to facilitate the filing of the agency, it is stipulated that the information that can be obtained through the government information sharing platform shall not be required to be repeatedly provided by the trademark agency.

"Cosmetic Production Quality Management Standard Inspection Points and Judgment Principles" will come into effect in December

The State Food and Drug Administration announced the "Cosmetic Production Quality Management Standard Inspection Points and Judgment Principles", which will come into force on December 1, 2022.

The "Principles" point out that for enterprises that are judged to have "defects in the production quality management system", the department in charge of drug supervision and management shall urge them to complete rectification within the specified time and submit a rectification report, and may organize on-site re-examination if necessary. For enterprises that are judged to have "serious defects in the production quality management system", the department in charge of drug supervision and management 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 suspend production and operation, and timely Control product risk. The enterprise shall complete the rectification within the specified time, and submit a rectification report to the department in charge of drug supervision and management. The department in charge of drug supervision and management shall conduct an on-site re-examination of the enterprise and confirm that the rectification meets the requirements before resuming its production and operation.

From December 1st, the "Certificate Documents for Exporting APIs to the EU" and the "Certificate for Drug Export Sales" officially launched electronic certificates

The State Food and Drug Administration announced that starting from December 1, 2022, electronic certificates will be used for the issued "Certificate Documents for Exporting Raw Drugs to the EU" and "Drug Export Sales Certificates". Electronic certificates have the same effect as paper certificates. Combined with my country's drug export work practice and the latest WHO guidelines, a new template for the "Drug Export Sales Certificate" was launched.

From December 15th, the Putonghua proficiency of elementary and middle school students will be divided into 6 levels

The Ministry of Education and the National Language Work Committee issued the "Primary and Middle School Students Putonghua Proficiency Test Grade Standards and Test Outline" (Trial), which divides the Putonghua proficiency of primary and middle school students into 6 levels, and stipulates the content, scope, test paper composition and scoring standards of the test, etc. , which is applicable to the assessment or evaluation and monitoring of the Putonghua proficiency of students in the fifth grade and above of the compulsory education stage. The specification will be implemented on a trial basis on December 15, 2022.