藥檢機構 的英文怎麼說

中文拼音 [yàojiǎnjīgòu]
藥檢機構 英文
drug control institutions
  • 藥 : Ⅰ名詞1 （藥物） medicine; drug; remedy 2 （某些有化學作用的物質） certain chemicals Ⅱ動詞1 [書面...
  • 檢 : Ⅰ動詞1 （查） check up; inspect; examine 2 （約束; 檢點） restrain oneself; be careful in one s c...
  • 機 : machineengine
  • 構 : Ⅰ動詞1 （構造; 組合） construct; form; compose 2 （結成） fabricate; make up 3 （建造; 架屋） bui...
  • 藥檢 : doping control testing
  • 機構 : 1 [機械工程] （機械的內部構造或一個單元） mechanism 2 （機關; 團體） organ; organization; institu...
  1. Use of banned drugs and methods is strictly prohibited in sports activities. institutions in charge of testing banned drugs shall conduct strict examination of the banned drugs and methods

    在體育運動中嚴禁使用禁用的藥物和方法。禁用藥物檢測機構應當對禁用的藥物和方法進行嚴格檢查。
  2. Wang, female, 34 years old individual does business the patient to tell infects the blister measles virus in 2002, the initial period has made some simple treatments, but whenever the month menstrual period manifests suddenly a time, the vulva ache, is rotten to the core, has the water blister, nearly soon loses the treatment the confidence, after afterwards saw we establish the gram china to promote the organization the advertisement, the order establishment gram kj medicinal preparation, the establishment gram takes orally series medicine and so on the capsule, after takes orally the external use 2 treatment courses, the symptom vanished, after stops the medicine to make two examinations in the local hospital the pure blister measles virus to transfer cloudyly, thoroughly convalesced, makes a follow - up visit, the observation after more than a year of, until now has not seen recurs, respent on the happy life

    王某，女， 34歲個體經商患者自述於2002年感染皰疹病毒，初期做過一些簡單的治療，但是每到月經期發作一次，外陰疼痛糜爛，有水皰，幾乎快要喪失治療的信心，后來看到我們安立克中國推廣機構的廣告后，訂購安立克kj劑，安立克口服膠囊等系列藥物，通過內服外用2療程后，癥狀消失，停藥后在當地醫院做了兩次檢驗hsv單純皰疹病毒轉陰，徹底痊癒，經過一年多的隨訪觀察，至今未見復發，重新過上了幸福的生活。
  3. Aqsiq requires that all processing plants producing poultry meat for export should establish ‘ five - unification ’ management system, i. e., unification of chick supply, unification of feed supply, unification of drug supply, unification of vaccination, and unification of slaughtering ; that all chicken for slaughtering must be from farms that have been put on file by supervision and quarantine authorities

    國家質檢總局規定：所有出口禽肉加工企業必須建立「五統一（即統一屠宰，統一供雛，統一供料，統一供藥，統一防疫） 」的管理體系，所屠宰的商品肉雞必須來自經檢驗檢疫機構備案的商品雞場。
  4. This microscope is provided with achromatic objectives, wide field eyepieces, abbe condenser, adjustable built ? in light source, and coaxial coarse and fine adjustment with focus stop. this microscope with his wide field eyepiece gives a nice and sharp image and is designed in a very modem way, it is designed for clinical experiments and classroom demonstration in medical and hygienic establishments, chemical laboratory, agricultural scientific research nets, research institutes and colleges as well as for the routine examination and research purpose in bioloy, bacteriology, cytology and pharmaceutical chemistry

    本顯微鏡採用消色差物鏡、廣角目鏡、阿貝聚光鏡，連續可調的人工光源及帶有限位置的同軸粗微動機構，視場廣闊、成象清晰、設計先進，可供醫療衛生機構、化學試驗室、農業科研系統、研究所及高等院校臨床試驗和教學示範，以及在生物學、細菌學、細胞學和藥物化學等領域作常規檢查和研究。
  5. During establishing domestic sickbed, check to other medical establishment, check, assay or need cure dispensation because of other disease, should make processing of average outpatient service, otherwise fund does not grant to pay

    設立家庭病床期間，到其他醫療機構檢查、復查、化驗或因其他疾病需醫治配藥的，應作普通門診處理，否則基金不予支付。
  6. Any unit or individual person shall not buy, sell, transfer or fraudulently use the bills, medicine bags, labels for pharmaceutical preparations, and medical documents such as medical record card, prescription pad, examination application, examination report, certificate of health examination, certificate of disease, birth certificate, death certificate, etc

    任何單位或者個人不得買賣、出借、轉讓或者冒用標有醫療機構名稱的票據、藥品分裝袋、制劑標簽以及病歷卡、處方箋、檢查申請單、檢查報告單、檢查證明書、疾病證明、出生證明或者死亡證明等醫療文件。
  7. Examine to violating collection the drug inspection agency with charge serious clue, cancel its examine qualification

    對違法收取檢驗費用情節嚴重的藥品檢驗機構，撤銷其檢驗資格。
  8. As part of the five - year plan to boost product safety, the government will build inspection offices at 16 ports, improve the regulatory facilities in the poorer central and western parts of the country and introduce rules that allow the regulator to shut factories suspected of making sub - standard goods

    作為《國家食品藥品安全「十一五」規劃》的一部分，中國政府將在16個口岸建立檢驗站，改善中國較貧困的中西部地區的監管設施，並制定相關法律法規，允許食品藥品監管機構查封涉嫌生產不合格商品的工廠。
  9. Because of the influences of the turbidity, ph of raw water, current, temperature and the pollutions of raw water, the process of coagulant dosage is a very complex reaction. to find out the automation of coagulant dosage and reduce the cost of the coagulant, many domestic and international scientific research organizations make research into the theory and mechanism of automation of coagulant dosage, such as the streaming current control method ( scd ), the emulation experimenting method in spot, mathematics model, flocculation control device ( fcd )

    由於受到原水濁度、 ph值、配水流量、原水溫度和其他水質污染的影響，投藥絮凝過程是一個非常復雜的反應過程，為實現投藥系統的自動化和降低混凝劑耗率，國內外相當多的科研機構和院校在進行投藥機理和自動化處理的研究，主要有流動電流儀檢測法（ scd ） 、現場模擬實驗法、數學模型、顯示絮凝控製法（ fcd法）等自動投藥方式的研究和實驗。
  10. Article 70 pharmaceutical supervisory and administrative departments and the pharmaceutical inspection institutions they have established, as well as the institutions exclusively engaged in pharmaceutical inspection they have appointed, shall not participate in pharmaceutical production and trade, and shall not endorse or supervise the production and sale of pharmaceuticals in their own names

    第七十條藥品監督管理部門及其設置的藥品檢驗機構和確定的專業從事藥品檢驗的機構不得參與藥品生產經營活動，不得以其名義推薦或者監制、監銷藥品。
  11. Research staff, persons in charge of pilot production, test, quality assurance and registration, heads of the organizations, keepers of the apis, samples, original records, files and credence, and finance staff should be on the inspection site and support the inspectors

    藥品研製過程所涉及的各試驗項目研究人員、樣品試制、檢驗、質量保證負責人、藥品注冊負責人、機構負責人、相關的原材料、樣品、各類原始記錄、檔案資料、票證憑據等的保管人員、財務人員在現場核查過程中應在崗，並按照現場核查人員的要求配合核查工作。
  12. Other major departmental components include the united states trustee, the office of the federal detention trustee ( ofdt ), the justice management division ( jmd ), the executive office for immigration review ( eoir ), the community relations service ( crs ), the office on violence against women ( ovw ), the national drug intelligence center ( ndic ), the office of the inspector general ( oig ), and several offices that advise the attorney general on policy, law, legislation, external affairs and oversight

    其他主要的組成部分包括反托拉斯司、司法管理司、移民檢查辦公室（ eoir ） 、社區關系司、施暴婦女辦公室、國家藥品智能中心（ ndic ） 、監察長辦公室（ oig ）和其他幾個為司法部長提供法律政策、立法、外部事務咨詢的機構。
  13. The drug control institution affiliated to the drug regulatory agency of the state council is responsible for standardizing the national drug standard substance and reference substance

    國務院藥品監督管理部門的藥品檢驗機構負責標定國家藥品標準品、對照品。
  14. Gathered the multitudinous iand development strength, the national new medicine clinical front security appraisal center the glp laboratory, the national clinical pharmacology base. in march, 2005, studies the association by the beautiful national essence lebanon gentleman microorganism usa wallless microorgamism reserch assoc. coordinated the union world venereal diseases research board, the international uropoiesis problem, becomes medicine which in the history first truly broke not governs discusses

    美國華黎士微生物研究協會usa wallless microorgamism reserch assoc . ，聚集了眾多國際領先的專家研究機構及全球頂尖學術專家及資深專業技術人員，協會匯集了58位國際權威的醫學性病專家及100名國際醫學專家學者，擁有世界最先進的病毒檢測設備及雄厚的技術研發力量國家新藥臨床前沿安全性評價中心glp實驗室國家臨床藥理基地。
  15. Through this tour, we find that canada has a complete set of veterinarian administration agencies and a sound legal system, disease control is orderly and effective, quarantine regulation is strict and well - placed, animal drugs are administered on a tight and standard basis, r d management is practical, lab animal safety level is high, and professional educational system is advanced

    通過此次考察，我們認為加拿大獸醫管理機構健全法律法規體系完善疫病控制有序有效檢疫監管嚴格到位獸藥管理嚴密規范行業協會作用明顯科研管理切合實際實驗室生物安全水平較高專業教育體系先進，確實為畜牧業良性有序發展起到了保駕護航作用。
  16. Any drug manufacturer to be established shall meet the following requirements : ( 1 ) stuffed with legally qualified pharmaceutical and engineering professionals and the necessary technical workers ; ( 2 ) provided with the premises, facilities, and clear environment required for drug manufacturing ; ( 3 ) having quality management and control units and personnel capable of quality management of and testing for drugs to be produced and the necessary instruments and equipment ; and ( 4 ) establishing rules and regulations to govern the quality of drugs

    開辦藥品生產企業，必須具備以下條件： （一）具有依法經過資格認定的藥學技術人員、工程技術人員及相應的技術工人； （二）具有與其藥品生產相適應的廠房、設施和衛生環境； （三）具有能對所生產藥品進行質量管理和質量檢驗的機構、人員以及必要的儀器設備； （四）具有保證藥品質量的規章制度。
  17. The drug quality control laboratories established or designated by drug regulatory agencies shall undertake the responsibility for drug testing required for conducting drug review and approval and controlling drug quality pursuant to the law

    藥品監督管理部門設置或者確定的藥品檢驗機構，承擔依法實施藥品審批和藥品質量監督檢查所需的藥品檢驗工作。
  18. The functionaries of pharmaceutical supervisory and administrative departments, of the pharmaceutical inspection institutions they established, and of the institutions exclusively engaged in the inspection of pharmaceuticals they appointed, shall not participate in pharmaceutical production and trade

    藥品監督管理部門及其設置的藥品檢驗機構和確定的專業從事藥品檢驗的機構的工作人員不得參與藥品生產經營活動。
  19. 5 undertaking the research and development for new medicine and the research relative to the drug quality. taking responsibility for guiding the low - ranking institutes for drug control to carry out their technical work, checking and evaluating their working quality and training their technical workers. according to the statistics, during 1985 2003, gxidc had finished the testing of more than 60 thousand drug samples, drafted and revised pieces of national drug standards and completed study projects of the research and development for new medicines and relative to drug quality added up to 538, started 35 technical training classes, published 360 research papers on national and provincial magazines and compiled 51 volumes of monograph

    我所於2000年2005年先後通過了綜合檔案省部級認證廣西技術監督局新一輪計量認證can及醫療器械和藥品包裝材料的監督評審擴項評審中國實驗室國家認可委員會認可cnal及藥品醫療器械藥品包裝材料檢測保健食品農藥殘留量生物製品蘇丹紅國家專項認可醫療器械食品化妝品的監督評審和擴項評審及出口新加坡中成藥中摻入違禁化學品檢測項目擴項認可，檢測能力現已達到447項國家食品藥品監督管理局醫療器械檢測機構資格認可。
  20. They are directed to government inspectors ? particularly those operating within small national regulatory authorities ( 1 ) ? to assist them in assessing manufacturers ' compliance with good manufacturing practices ( gmp ) ( 2 )

    它主要用於指導藥政部門的檢查官，特別是那些在小型藥政機構工作的人員，幫助他們判斷制藥企業是否符合gmp的要求。
分享友人
分享到 Line

分享到臉書