法定藥品 的英文怎麼說

中文拼音 [fǎdìngyàopǐn]
法定藥品 英文
official drug
  • 法 : Ⅰ名詞1 （由國家制定或認可的行為規則的總稱） law 2 （方法; 方式） way; method; mode; means 3 （標...
  • 定 : Ⅰ形容詞1 （平靜; 穩定） calm; stable 2 （已經確定的; 不改變的） fixed; settled; established Ⅱ動詞...
  • 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...
  • 法定 : legal; statutory法定安培 legal ampere; 法定貶值 official devaluation; 法定標準 statutory standard...
  • 藥品 : drug; medicinal; medicines and chemical reagents; pharmaceutical
  1. The pharmacy and poisons board ( ppb ) is the statutory authority set up under the pharmacy and poisons ordinance to take charge of the registration of pharmaceutical products in hong kong

    藥劑業及毒藥管理局是根據《藥劑業及毒藥條例》 （ 《條例》 ）的規定而成立的法定機構，負責處理本港藥劑製品的注冊事宜。
  2. Standard test method for evaluation of first aid antiseptic drug products

    評定急救抗菌藥品的標準試驗方法
  3. Chinese title, english title, author, the affiliation and address of the first author, journal title, publication year, volume, issue, page, publication type, check tag, history of medicine, grant type, subject headings, classification code, language, chinese abstract, english abstract, animal variety, dosage forms, pharmacology of chinese herbs, pharmacology, name of disease, diagnosis standard, pathogenesis, trial type, treatment of disease, name of drug and formula, chemical name of medicines, english name of medicines, ingredients and dosage of formula, drug compatibility, usage and dosage, acupuncture and tuina points, acupuncture and tuina manipulation, side effect, therapeutic effect guideline, result of cure, materia medica, chemical structure, physical and chemical properies, effective component, chinese medicine identification, method of processing, pharmaceutical techniques, medicinal action and pharmacological effect, pharmacokinetics, and toxicology

    中文文題、英文文題、作者、第一作者單位、第一作者所在地、期刊名稱、出版年、卷、期、頁碼、文獻類型、特徵詞、醫學史、資助類型、主題詞、關鍵詞、分類號、語種、中文文摘、英文文摘、動物品種、劑型、中藥藥理、西藥藥理、疾病名稱、診斷標準、疾病機理、試驗方法、疾病治療、藥名方名、化學藥名、英文藥名、組成劑量、藥物配伍、用法用量、針推穴位、針推方法、不良反應、療效指標、療效結果、藥材學、化學結構、理化性質、有效成分、中藥鑒定、炮製方法、制藥工藝、藥物作用與藥理效用、藥代動力學、毒理學。
  4. Plastics - determination of the effects of liquid chemicals including water

    塑料耐液體化學藥品包括水性能測定方法
  5. Standard test methods for rubber chemicals - determination of percent insoluble sulfur by solvent extraction

    橡膠加工用化學藥品.用溶劑提取法測定不溶解硫磺百分比的標準試驗方法
  6. The japanese pharmacopoeia ( jp ) was designated as the official japanese drug standard by the pharmaceutical administration law of japan

    日本藥局方》 （ jp ）是日本《藥事法》中規定的日本藥品的法定標準。
  7. Suggestions in this paper include stepped - up lawmaking, standardization of leechdom production and circulation, strengthening the management of listed hospitals and perfecting construction of networks

    本文提出了加快立法，規范藥品生產、流通環節，並強化定點醫院管理和網路系統建設等建議。
  8. The drugs listed in article 10 shall pass through the ports with a special approval of the state, permitting the entry of imported drugs

    其中本辦法第十條規定情形的藥品，必須經由國家特別批準的允許藥品進口的口岸進口。
  9. 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。
  10. Operating methods for the tests and assays of drugs. part 6 : biological assays of drugs

    藥品檢驗操作規程.第6部分:藥品生物測定法
  11. 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。
  12. In the present ten years, domestic biochip technique has been developed enormously, and applied to many fields, such as life science research diagnosis, new drug development, bio - weapon war, judicial evaluation, foods and environment supervise etc. however, the biochip analyzer, which is one important part of biochip technique, is almost all depended on foreign ones

    近10多年來，國內生物晶元技術的發展備受矚目，在生命科學研究、疾病診斷、新藥開發、生物武器、司法鑒定、食品衛生監督等等領域已越來越被廣泛運用。然而在生物晶元技術中的重要組成部分之一? ?生物晶元的檢測設備卻幾乎一直依賴國外的產品，其壟斷性的昂貴價格，加上復雜的專業分析操作，對我們生物晶元的應用推廣造成了許多障礙。
  13. 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。
  14. 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。
  15. 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。
  16. Operating methods for the tests and assays of drugs. part 4 : determination of residual organic solvents

    藥品檢驗操作規程.第4部分:有機溶劑殘留量測定法
  17. Most republicans opposed the bill, many saying it is unnecessary because private insurers and others have already succeeded in extracting favorable price deals from drug companies

    大部分共和黨人反對此法案，稱這是不必要的，因為私人保險及其它已經與藥品公司商定了一個合理的價格。
  18. 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。
  19. While warnings are often appropriate and necessary - the dangers of drug interactions, for example - and many are required by state or federal regulations, it isn ' t clear that they actually protect the manufacturers and sellers from liability if a customer is injured

    雖然警告常常是恰當而且必要的-例如，藥品互相作用的危險-並且不少還是州或聯邦條例所要求的，但是如果顧客受傷，它們是否確能保護製造商和銷售商免於法律責任，還不一定。
  20. 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。
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