管制藥品管理 的英文怎麼說

中文拼音 [guǎnzhìyàopǐnguǎnlǐ]
管制藥品管理 英文
dea drug enforcement adminestration
  • 管 : Ⅰ名詞1 （管子） pipe; tube 2 （吹奏的樂器） wind musical instrument 3 （形狀似管的電器件） valve;...
  • 制 : Ⅰ動詞1 （製造） make; manufacture 2 （擬訂; 規定） draw up; establish 3 （用強力約束; 限定; 管束...
  • 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...
  • 品 : Ⅰ名詞1 （物品） article; product 2 （等級; 品級） grade; class; rank 3 （品質） character; qualit...
  • 理 : Ⅰ名詞1 （物質組織的條紋） texture; grain （in wood skin etc ） 2 （道理;事理） reason; logic; tru...
  • 管制 : 1. （強制管理） control 2. （對罪犯強制管束） put under surveillance
  • 藥品 : drug; medicinal; medicines and chemical reagents; pharmaceutical
  • 管理 : manage; run; administer; supervise; rule; administration; management; regulation
  1. The speciality of chinese traditional medication decoction pieces means the hard job of its quality controlling and management, which covers identification of the confusion, falsify and counterfeit, checking of medicate part, impurity, humidity, bitten by insect, mustiness and oil - releasing, counting of package and number, and the quality controlling and storing management in warehouse. the author here would like to share some experiences which from both theory and the practices

    中藥飲片的特殊性決定了其質量控制和管理的難度，從飲片入庫前的驗收，包括易混品、摻偽品、假冒品的鑒別，藥用部位、飲片雜質、濕度、蟲蛀、發霉和走油等方面的檢查，及包裝和數量的清點，到飲片的在庫養護如庫房的管理和飲片的保存等，都需要在實踐中結合理論進行摸索和總結。
  2. Dtc is a licensed by national agency for food, drug administration and control ( nafdac ) to carry on the business of producing drinking water under the registered “ vallon ” trademark in different quantities amongst other businesses

    Dtc是在國家食品與藥品管理控制局（ nafdac ）許可下可以生產其一：商標為「 vallon 」的不同質量層次的飲用水。
  3. In addition, certain food shipments that are re - exported, and shipments containing meat, poultry, and egg products falling under exclusive usda jurisdiction, are exempt. additional exclusion criteria can be found at the fda web site

    此外，由美國農業部（ usda ）管制下的須按照美國農業部相關條例和法規操作的肉、禽、蛋製品和再次出口的食品也除外。附加的免除信息可見美國食品及藥品管理局網站，網址
  4. Article 1 for the purpose of strengthening the administration of accredited supervisors and regulating their behaviors of on - the - spot supervision and inspection over drug production, these provisions are formulated in accordance with the relevant provisions of the pharmaceutical management law and other related provisions on drug manufacturing supervision and management

    第一條為進一步加強對派駐監督員的管理，規范其藥品生產現場監督檢查行為，根據《藥品管理法》以及藥品生產監督管理的有關規定，制定本規定。
  5. Taiwan biotech was able to implement asuccessful diversification of its product line. the company also experienced significant improvements in its management systems and operational efficiency. as a result, not only did taiwan biotech achieve major breakthroughs in r d, it was able to complete production process development for three generic drugs within two years, allowing the company to move successfully into international markets

    初期佑益生技的原料藥生產集中於抗生素，在張副總的專業考量下，基於市場考量，佑益生技在研發方向作了大幅的修正，朝相對競爭性較小的非抗生素領域發展，並進行產品多樣化發展此外張副總更在制度管理和執行效率上進行改善，致使益佑生技在原料藥的技術研發方面有重大突破，在兩年內完成三種generic原料藥產品的製程開發，面向國際市場。
  6. Article 55 for pharmaceuticals controlled by the fixed and directive pricing system of the government, the competent authority of pricing of the government shall fix and adjust the price with reason in conformity with the principles for fixing prices as prescribed by the price law of the prc and according to the considerations of societal average costs, market supply and demand, and the level of societal tolerance to achieve accord between quality and price, to avoid excessive prices, and to safeguard the due interests of the users of the pharmaceuticals

    第五十五條依法實行政府定價、政府指導價的藥品，政府價格主管部門應當依照《中華人民共和國價格法》規定的定價原則，依據社會平均成本、市場供求狀況和社會承受能力合理制定和調整價格，做到質價相符，消除虛高價格，保護用藥者的正當利益。
  7. Method according to instructive rules of productive quality and standard of management of chinese medical materials ( gap ), to control various kinds of factors which influent desmodium styracifolium ( osb. ) merr quality

    方法以國家食品藥品監督管理局發布的《中藥材生產質量管理規范》 （ gap ）為指導原則，控制影響廣金錢草質量的各種因子。
  8. 4 canadian tas from cfia and 5 chinese experts from moh, aqsiq, and sfda had been invited to give presentation about nutritional labeling, food recall, risk assessment and analysis, food contamination monitoring and reporting

    會議邀請了加拿大食品檢驗署的4位專家和質檢系統衛生系統及食藥總局系統的5位中方專家就食品召回的風險分析和制度建立食品營養標簽，食品安全風險分析管理，以及食品污染監測和報告等方面開展培訓。
  9. In january 1993, china exercised control over the export licenses for the 22 precursor chemicals as listed in the un convention against illicit traffic in narcotic drugs and psychotropic substances, and in june 1996 it also exercised control over the import licenses for these chemicals

    1993年1月，中國對《聯合國禁止非法販運麻醉藥品和精神藥物公約》所列舉的22種易制毒化學品實行出口許可證管理； 1996年6月，又規定對上述22種易制毒化學品實行進口許可證管理。
  10. And use some theories about marketing channel construction and management, containing relationship marketing theory, supply chain theory, channel authority transfer theory, stimulating theory and game theory, analyze the macroscopic and microcosmic change of the whole medicine industry, and find out the opportunities in the market and challenges confronted with. through analyzing the macro and micro environment of the whole medicine industry, studying the development of medicine industry marketing channel - model and the feature of update model, relating with the experience of the same company ' s channel construction, the author study the xiamen meacon co. with realizing its marketing channel actuality, using swot analyse way, analyze its features and problems

    本論文採用實證研究法、深度訪談法、定性與定量相結合的方法，運用營銷渠道構建及管理的相關理論，包括關系營銷理論、供應鏈理論、激勵理論、渠道權力轉移理論以及博弈論等理論，通過分析整個醫藥行業的宏觀和微觀環境變化，研究醫藥市場營銷渠道模式演變過程和現有模式的特點，並結合相同類型企業渠道建設的經驗，針對廈門美康制藥公司的營銷渠道的現狀，分析其特點以及存在的弊端，並根據消費品營銷渠道一般模型，提出了其營銷渠道框架的重構方案，即美康公司四級營銷渠道的構建方案。
  11. 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。
  12. A licence is required to import, export, supply, procure, deal in or with, possess or manufacture controlled chemicals. to fulfill an international obligation under the united nations convention against illicit traffic in narcotic drugs and psychotropic substances, 1988, government of hksar introduced control on 25 chemicals which can be used for the manufacture of dangerous drugs or psychotropic substances

    進出口、供應、獲取、經營、處理、管有或製造受管制化學品須領有牌照。為履行1988年聯合國禁止非法販運麻醉藥品和精神藥物公約規定的國際義務，香港政府對25種可以用於製造危險藥物或精神藥物的化學品實施管制。
  13. Methods : basis 《 the drugs management method 》, 《 the drugs register to manage the way 》 ( try the line ) and 《 the medical treatment organization product registers to manage the way 》 ( try the line ) of provision, the basic theories of the application chinese medicine medicine, carried on the study to path and methods of the new medicine a research of chinese herbal medicine

    方法：依據《藥品管理法》 、 《藥品注冊管理辦法》 （試行）和《醫療機構制劑注冊管理辦法》 （試行）的規定，應用中醫藥的基本理論，對規范研製中藥新藥新制劑的途徑和方法進行了探討。
  14. In this paper, the drug administration system is researched and devoloped. carring out computer based management, the drug information in a hospital is completely brought into the hospital information as a real time situation with high share and high efficiency. this paper introduces the features, dafabase, techmical process and basic functions of the drug administration system

    為加強醫院的藥政管理工作，開發了醫院藥政管理系統，並且實施聯網管理，將醫院藥品信息全面納入到醫院信息總體管理中，最終使藥品信息處于高度共享、高效率的實時處理狀態，形成從總體調控到相互制約的管理體系，以確保醫院獲得良好的效益。
  15. It causes a feeling of excitement, said liu. in tests conducted on animals they increase their activity, running and jumping aimlessly

    管制藥品管理局柳家瑞：有興奮的效果，做動物實驗可以看到， ?的活動比較增加，會跑來跑去，跳躍的方式。
  16. Scp musculus chondroitin series products, which new fine bio - tech cosmetic technological cooperates with wonderful l. l. c., were applied for fda certify in the end of 2006, and have already passed in february 2007

    新優生化科技與美國wonderful l . l . c .公司技術合作之專利產品scp藍肽肌活系列scp musculus chondroitin ，已於2007年2月通過fda美國食品暨藥物管理局審核，取得制售證明。
  17. Scp series were expected to pass usfda s examine the scp series products, which were made by new fine and authorized from wonderful l. l. c. usa, were sent to usfda and expected to pass the examine in the early 2007

    新優生化科技與美國wonderful l . l . c .公司技術合作之專利產品scp藍肽肌活系列scp musculus chondroitin ，可望於2007年初通過fda美國食品暨藥物管理局審核，取得制售證明。
  18. Congress told the agency in 1994 it must issue a regulation tightening federal safety standards on dietary supplements. the industry reacted favorably to the new rule

    美國國會在1994年就敦促美國食品及藥物管理局發布食品安全法規，以加強膳食添加劑的控制。業內對此項新規定表示支持。
  19. It said it supported food and drug administration ( fda ) standards and that the recent recalls proved that the current regulatory system protected consumers. “ consumers can remain confident in making bottled water their beverage of choice

    協會指出，協會始終堅持美國食品及藥物管理局所規定的標準，而最近公開收回的出廠產品也證明了現行的管理機制隊消費者是有保障的。
  20. These include increasing access to water, sanitation and energy ; achieving sustainable fisheries ; halting the loss of biodiversity both on land and in our oceans ; better chemicals management ; increased use of renewable energy, and increased energy efficiency

    這些承諾包括增加使用水、衛生設施和能源的機會；建立可持續漁業；制止陸地和海洋多樣性的喪失；改善化學藥品管理；提高可再生能源的使用和提高能效。
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