Category | Announcement No. | Comments |
Health Quarantine | Announcement No.91 of 2019 of the General Administration of Customs | Vehicles, containers, goods (including corpse bones), luggage, mail and express mail from the Republic of Congo must be subject to health quarantine If mosquitoes are found in the quarantine inspection, they shall be subject to health treatment in accordance with regulations. The announcement will take effect on May 15, 2019 and will be valid for 3 months |
Administrative Approval | Announcement No.92 of 2019 of the General Administration of Customs | Announcement on publishing the list of designated regulatory sites for imported edible aquatic animals. This announcement will add one designated regulatory site for edible aquatic animals within the jurisdiction of Tianjin Customs and Hangzhou CustomsRespectively. |
Customs Clearance | Announcement No.87 of 2019 of the General Administration of Customs | 1. The exemption conditions applicable to the announcement are spare parts and products directly required for the maintenance purpose of the end user. 2. The applicable product range refers to the import of vehicle maintenance parts with HS of 870821000, 870829410 870829400,870839900,870830900,870830900,870830900,870830900,870830900,870830900, 870830990,8708995900.3 Importing enterprises are allowed to make
customs declaration first based on the Self-declaration of Exemption from Compulsory Product Certification. Key points for attention, import enterprises must obtain the Exemption Certificate” and enter it into the declaration system within 14 days from the date of declaration of the means of transport. Four, the customs on the basis of the “self declaration “after the declaration, the declaration form to amend the way to record information, not to record customs declaration errors: Review and correct customs declaration error records shall not be used as records for the customs to identify the credit status of enterprises |
Customs Clearance | No.102 (2019) of the State Administration of Market Supervision | Market supervision departments at all levels (including dispatched offices) are required to be responsible for the supervision and inspection of the following areas: 1. Carry out supervision and inspection of certification bodies, mandatory designated certification bodies for products and designated laboratories (hereinafter referred to as certification bodies) to investigate and deal with illegal acts of certification bodies: 2, to carry out supervision and inspection of the practice of certification practitioners, responsible for investigating and dealing with illegal acts of certification practitioners: 3, to carry out supervision and inspection of certification certificates and certification marks responsible for investigating and dealing with illegal acts of certification certificates and certification marks; 4, to carry out supervision and inspection of compulsory product certification (hereinafter referred to as CCC certification) activities, responsible for investigating and dealing with violations of ccc certification; 5, to carry out supervision and inspection of organic product certification activities, responsible for investigating and dealing with illegal acts of organic product certification: 6, accept complaints and reports on certification activities and deal with them according to law: Responsible for supervision of other certification activities and investigation of certification violations. The provincial market supervision departments shall submit the supervision work to the General Administration beforeDecember 1 of each year. |
Decree No.9 of the State Administration of Market Supervision and Administration was Promulgated | The “Measures for the Administration of Imported medicinal Materials” implements classified administration of first-time imported and non-first-time imported medicinal materials. The examination and approval of the first importedmedicinal materials shall be entrusted to the provincial drug supervision and administration department where the applicant is located. The sample inspection originally undertaken by the China Food and Drug Administration Research Institute shall also be adjusted to the provincial drug inspection agency accordingly. To simplify the import management of non-first imported medicinal materials, the applicant can go directly to the port or the department in charge of drug supervision and administration at the border port for the record and handle the import drug customs declaration form. The” measures” shall be implemented as of January 1, 2020 | |
State Administration of Market Supervision No. 44 of 2019 | It is clear that the original research drugs of the same enterprise that have been approved for import registration or clinical trials in China are imported once as reference drugs for clinical research of biological similar drugs | |
The State Administration of Market Supervision No.45 of 2019 | Announcement on Relevant Issues Concerning the Approval of Implementation of Extension Commitment System for Special Use Cosmetics Administrative License. The announcement will come into effect on June 30, 2019. Key points: First, by optimizing the renewal process of administrative license for special purpose cosmetics, the efficiency of review and approval will be further improved; The second is to further consolidate the main responsibility for quality and safety of enterprises by specifying and clarifying the self-inspection requirements of enterprise products. Third, it is clear that if the license is not renewed, the products shall not be produced or imported from the date when the validity of the license expires, and the law enforcement requirements shall be uniformly supervised | |
Food Safety Committee of the State Council No.2 of 2019 | Notice on Issuing the Key Work Arrangements for Food Safety in 2019. The implementation of imported food door guard” action. We will continue to push forward the “Safe Project for Imported and Exported Food vigorously crack down on food smuggling and prevent the safety risks of imported food. We will promote the construction of a good faith system, include import and export food enterprises in the import and export credit management of customs enterprises, and jointly punish those who have seriously broken their promises | |
National Nuclear Safety Administration, No. 126 of 2019 | Notice on Approving the Use of NPC Transport Containers in the People’s Republic of China) NPC transport containers manufactured by US Global Nuclear Fuel CO., Ltd. are allowed be used in China. The design approval number is CN/006/AF-96 (NNSA). The approval period is valid until May31, 2014. | |
General | No.3 of 2019 of the State Food and Material Reserve Bureau | Since December 6, 2019, 14 recommended industry standards such as “Camellia oleifera seeds”, “Paeonia suffruticosa seeds for oil, “Juglans regia seeds for oil” and “Rhus chinensis seeds” will be implemented |
Post time: Dec-19-2019