Customs clearance requirements and customs clearance port
First of all, let's take a look at the customs clearance requirements for imported drugs, China's imported drugs control regulations by the "Chinese People's Republic of China *** and the State Drug Administration Law" to determine the thirty-nine provisions of the drug importation, must be organized by the State Council drug supervision and management department to review the examination of the examination confirmed that meets the quality standards and safety and effectiveness before approval. Effective, before the approval of the import, and issue a certificate of registration of imported drugs. Article 40 provides that drugs must be imported from the ports that allow the import of drugs, and imported drugs by the enterprise to the port where the supervision and management department for the record, the Customs and Excise Department with the drug supervision and management department issued the "Imported Drugs Customs Clearance Order" release. The port where the drug supervision and management department shall notify the drug testing organizations in accordance with the provisions of the State Council drug supervision and management department of the imported drugs for sampling and testing. At present, there are 19 cities that allow the importation of medicines, namely Beijing, Tianjin, Shanghai, Dalian, Qingdao, Chengdu, Wuhan, Chongqing, Xiamen, Nanjing, Hangzhou, Ningbo, Fuzhou, Guangzhou, Shenzhen, Zhuhai, Haikou, Xi'an and Nanning. For biological products and the first time in China's domestic sales of drugs and other drugs specified by the State Council, there are three designated ports of entry: Beijing, Shanghai and Guangzhou. In addition to the above ports, in order to solve the border trade demand for imported medicines, there are 20 border ports as Chinese herbal medicine customs clearance ports, by the corresponding border ports of the Drug Inspection Institute is responsible for the inspection of the 20 ports are Heilongjiang Province, Heilongjiang Heilongjiang Province Heihe, Dongning, Jilin Province, Ji'an, Changbai, Tumen, Samhain, the Inner Mongolia Autonomous Region, Erlianhot, Manchuria, Guangxi, Pingxiang, Dongxing, Longbang, Yunnan Province, Ruili, Tianbao, Jinghong, Hekou, Xinjiang Alashankou, Horgos, Turgut, Hongqilav, Tibet Autonomous Region Zhangmu. It is worth noting that the recent Hainan to introduce a new measure, according to the provisions of the imported drugs from the port of Hainan Free Trade Port allows the import of drugs imported into the port of medicine, to the port where the drug supervision and management department for the record, without having to deal with imported drugs, customs clearance cell phone without having to check the imported drugs customs clearance form. But the provisions of the current stage of consultation with the community, to the real implementation should take a long time. In addition to conventional drugs, radiopharmaceuticals must be imported in line with China's drug standards or other medicinal requirements, and in accordance with the provisions of the Drug Administration Law to obtain a certificate of registration of imported drugs. Import of narcotic drugs and psychotropic substances within the scope of national regulations, must hold the State Council Drug Administration issued the "Import Permit" and "Export Permit".Pharmaceutical import and customs clearance application process
First of all, the importer needs to have certain enterprise qualification requirements, including: First, import and export business rights; Second, the business license business scope of the Chinese herbal medicine or important drinks; Third, the "imported drugs registration certificate", "production license" or "business license"; Fourth, the Customs and Excise Department signed a paperless contract, customs Enterprise Annual Report declaration, electronic commissioning agreement signing (import processing); five, the need for approval Secondly, the need to submit the customs declaration information are: 1 , imported medicinal materials application form; 2 , the applicant's production license or a copy of the operating license, the applicant is the holder of a listed pCm license, should provide a copy of the relevant documents to prove the approval; 3, a copy of the exporter's main registration documents; 4, a copy of the purchase contract and its instruments; 5, the ecology of the origin of the medicinal herbs, resource reserves, wild or planting and breeding conditions, harvesting and processing of the origin of the information; 6, the medicinal herbs and the origin; 7, the territory of the animals and plants with a qualification of the identification of the origin of the county's institutions containing the basis for identification 7, by the territory of the animal, plant origin identification qualifications of the agency issued by the county containing identification basis, identification conclusions, sample pictures, identifiers, identification agencies and their official seal and other information of the original identification of the base of the original certificate of the medicinal herbs. Finally, the specific process is as follows: 1, imported medicines after signing the contract, payment of remittances and pick up the goods, export customs clearance, sent by air or sea to the domestic ports of imported medicines customs clearance, customs clearance and then transportation and distribution to the destination. Before the goods arrive at the port you need to prepare all the import customs declaration information, otherwise there will be a lot of additional costs, and the time is slow. 2, the provincial Drug Administration will review the application in accordance with the law, has canceled the declaration of documents in the original verification, changed to network review. Applicants to submit proof of class declarations should be the original or stamped with the official seal of the photocopy of the electronic material, other declarations should be stamped with the official seal of the electronic material. 3, the Provincial Drug Administration through the online approval system to the applicant to issue corrective materials, acceptance, inadmissibility and other electronic notification. In the system prompted the end of the approval, the applicant can be in accordance with the requirements of the announcement of the results of the approval, sent by mail or to the provincial government service center window to get the results. I believe that many people see here, has been dizzy, drug import customs clearance procedures are complex, need to provide a lot of information, the average person is difficult to prepare all, so there is no easy way to do it? Some people will choose to clear customs from Hong Kong, and then send the drugs to the destination. Hong Kong is a free port, the general import or export of goods are not required to pay any import tariffs, and there are no tariff limits or additional taxes. There is also no value added tax or general service tax. Customs clearance procedures are simpler than those in the Mainland and can be done electronically. For customs clearance, you only need to provide: manifest; copy of detention notice; bill of lading, air waybill or other documents; invoice, packing list; and other documents such as import license, removal permit, etc. Although the process is simplified, but still need to provide a lot of information, for ordinary people, is still not so convenient. In contrast, Hong Kong Jiemin Pharmaceuticals one-stop service is much more convenient, eliminating the lack of qualifications, missing documents, the process is not familiar with a variety of trouble. Jinmin (Hong Kong) Pharmaceutical Co., Ltd. was formerly known as the Southern Pharmaceutical Foreign Trade Co. The company's business mainly focuses on the import and export of pharmaceutical products, one-time import, import of clinical study control drugs, and so on. Ltd. is licensed by the Department of Health of Hong Kong to import all types of pharmaceutical products, including comparator drugs, specialty medicines, orphan drugs, clinical trial supplies, oncology medicines that are not available in the market, medicines that are unregistered or unregistrable, and special medicines that are required by patients. Specialty medicines requested by patients (with a doctor's written authorization), urgent medical needs, emergency medicines, and so on. The company has the ability to take photographs of medicines, store and wholesale medicines, purchase medicines for private clinics, hospitals, governmental organizations and even pharmacies, and apply to the government for importation of medicines needed by patients. If you are in urgent need of drugs and can not go through the import customs clearance route, you may want to go to Hong Kong Jiemin Pharmaceuticals to seek help, save time and effort.