藥品信息管理 的英文怎麼說

中文拼音 [yàopǐnxìnguǎn]
藥品信息管理 英文
drug information management
  • : 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...
  • : Ⅰ名詞1 (物品) article; product 2 (等級; 品級) grade; class; rank 3 (品質) character; qualit...
  • : Ⅰ名詞1 (呼吸時進出的氣) breath 2 (消息) news 3 (利錢; 利息) interest 4 [書面語] (子女) on...
  • : 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;...
  • : 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...
  • 藥品 : drug; medicinal; medicines and chemical reagents; pharmaceutical
  • 管理 : manage; run; administer; supervise; rule; administration; management; regulation
  1. Development and building of information system of stupefacient and chlorpromazine management

    麻醉和精神藥品信息管理系統的開發與構建
  2. Building of mis on medicine raw materials sales

    原料銷售系統的構建
  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 )制下的須按照美國農業部相關條例和法規操作的肉、禽、蛋製和再次出口的食也除外。附加的免除可見美國食局網站,網址
  4. Hospital information system and doctor protect effective interface of system implementation, and has promoted the quantity management and popularization that doctor ' s work is stood of drug, and has reduced the cocurring rate of wrong prescription, and make the hospital serve more smooth and easily

    原因系統與醫保系統實現有效介面,促進了的數量和醫生工作站的推廣,降低了錯誤處方的發生率,使醫院服務更加順暢。
  5. This paper researched on quality management of material flow of pharmaceuticals manufacturing based on the investigation of small and medium pharmacies, and emphasis on two aspects : information integration and risk analysis of material or product confusion. 1

    本論文通過對中小型生產企業的深入調研,研究了生產物流過程質量方法,其中重點對集成和混批混料風險分析兩個方面進行了深入研究: 1
  6. 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

    為加強醫院的工作,開發了醫院系統,並且實施聯網,將醫院全面納入到醫院總體中,最終使處于高度共享、高效率的實時處狀態,形成從總體調控到相互制約的體系,以確保醫院獲得良好的效益。
  7. Software & integrated circuit industries : data - base, platform software such as network administration software, middleware, network security software, embedded software, oa, erp, financial software, crm, scm, eam, system & security software, electrical automatization software, corporation informatization and e - government software, telecom and financial stock software, multimedia education software, service industry software, firewall, cartoon game, education software, medical treatment software, production of integrated circuit, all kinds of industry solution, etc

    軟體與集成電路產:數據庫、網軟體等平臺軟體,中間件、網路安全等中間軟體,嵌入軟體、 oa 、 erp 、財務軟體、 crm 、 scm 、 eam 、系統與安全軟體、電力自動化行業應用軟體、企業化與電子政務軟體、電金融政券軟體、圖書軟體、稅務行業軟體、通行業軟體、政府辦公軟體、數據存儲軟體、多媒體教學軟體、服務行業軟體、防火墻、動漫遊戲、教育軟體、醫業行業軟體、醫療軟體集成電路產及各種行業解決方案等。
  8. Theresult we through the optimized administration examination andapproval, the production management quality control standardauthentication, to the drugs and the instrument not good responded themonitor started, promoted our country medicine retail marketdevelopment, but our country medicine supervised the management alsoto have the medical establishment system not not perfectly, the ruralmarket drugs supply and sales channel chaotic, the drugs not goodreaction reactivity rate is not real and so on some questions, weshould open up the supervising and managing domain, enhanced thesupervising and managing potency, the unified plan and organizes theinformation examination, drugs supervising and managing to put withemphasis on the countryside basic unit drugs market, furtherconsummated our medicine to supervise the management system managementsystem

    結果我們通過優化行政審批、生產經營質量規范認證、對與器械不良反應監測啟動,促進了我國醫零售市場的發展,但我國的還存在醫療機構體系不健全、農村市場供銷渠道混亂、不良反應率不真實等一些問題,我們應該拓寬監領域,提高監效能、統一規劃和組織化稽查、重點放在農村基層市場,進一步完善我們的系統。
  9. New u. s. food and drug administration ( fda ) regulations, issued under the " bioterrorism act ", require food shippers to provide additional information to clear u. s. customs

    根據美國食局( foodanddrugadministration ,簡稱fda )按照「生物恐怖主義法案」 ( bioterrorismact )頒布的新規定,食發貨人在美國海關辦清關手續時須提供附加
  10. In order to promote the the medical treate insurance reform, protect the benefit of the patient participating the the medical treate insurance, offer the convenience for the medical treate insurance patient, and avoid the repeated investment, improve the information level and the hospital management, we develop the management information system containing the insurance and the own ' s expenses 0 the system bring about the settle accounts with medical treate insurance management centre 0 the whole information system implements the the hospital whole business flow, according to the our country system framework mode, management mode, management programmer and the medical treate insurance relevant policy. this system have the below modual, the subprogram of the procedure transacting to be in hospital, then subprogram of doctor ' s advise management, the subprogram of charging in the hospital, the subprogram of patient district of durg - store, the subprogram of the surgery section office, the subprogram of the anesthesia section office, the subprogram of sumedicial records, the subprogram of comminuction with the medical treate insurance management centre 0

    醫院在日常中,存在兩條主線,一是患者,一是財務。本子系統圍繞患者看病時資金的流動展開?從入院到交預交款,、處置的費用,直至醫院內部的二級核算(科室核算、醫師核算) ,都應有據可查,最重要的是能及時抽出財務報表,與醫保中心清算,同時按照國家衛生部頒發的標準為醫院提供相應報表,供財務核算以及掌握醫院整體。整個系統根據我國現行體系結構模式、模式和程序以及醫保的相應政策、按照職能分工劃分為門診、住院、、醫技、財務、行政等各個相關聯的部分加以結合,實現醫院整體的業務流程。
  11. For more information on genomics, please see the 2005 fda consumer magazine article " genomics and personalized medicine.

    有關基因組學的更多,請查看《 2005食局消費者雜志》中文章《基因組學和個性化用》 。
  12. With economic globalization and the arrival of the information era, the world ' s enterprises are faced with more severe challenges and competition in the market, the domestic pharmaceutical companies as well. on the one hand between the restructuring of enterprises, relative to the survival of small enterprises facing pressure ; on the other hand, how to make better products faster occupied market, gave domestic pharmaceutical enterprises to adapt and make higher demands on competitiveness

    隨著經濟全球化和時代的來臨,世界各國的企業都面臨著更加嚴峻的市場競爭和挑戰,國內的制企業也是如此,一方面企業間的重組,使相對弱小的企業面臨著生存的壓力,另一方面怎樣使產更快更好地佔領市場,都給國內制企業的競爭能力和水平提出了更高的要求。
  13. Under modern management, the qingping markt is also internationally known as a self - branded tcm trading centre for e - commerce, information, logistics, testing and verification as well as national medicine exhibition

    清平中材專業市場也是國際上知名、具有自主牌和商標的、功能齊全、現代化的中材交易采購中心、電子商務和查詢中心、物流中心、檢驗和鑒證中心以及國匯展中心。
  14. According to the problems existed in present pharmaceutical sale system and realize the following aims : ( 1 ) realizing the share of information and timely exchange between enterprises and customers, and shortening commodities provision cycle ; ( 2 ) optimizing enterprises " business process, increasing enterprises " working efficiency and reducing workers " labor load ; ( 3 ) establishing enterprises " efficient information network and making decision - makers master enterprises " operation timely and control it efficiently ; ( 4 ) providing strong auxiliary support for enterprises " operation analysis and decision and making enterprises " decision quick, scientific and effective ; ( 5 ) reasonable classifying customer management, shortening response time, increasing service quality and reducing enterprises " operation cost

    該文章根據目前醫銷售系統存在的問題,採用delphi作為技術平臺,開發出適合現階段醫企業的客戶系統,實現了以下幾個目標: ( 1 )實現企業與客戶之間的共享和及時交換,縮短商供貨周期。 ( 2 )對企業的業務流程進行全面優化,提高企業辦公效率,降低工作人員的勞動負荷。 ( 3 )建立企業有效的網路,使決策者能夠及時掌握企業的運營,進行有效的控制。
  15. Records of software validation should be maintained by the drug establishment, although when conducted by outside experts such records need not be voluminous but rather complete enough ( including protocols and general results ) to allow the drug manufacturer to assess the adequacy of the validation

    雖然軟體驗證的記錄應該由公司保存,但當外界專家這些記錄時可以不必有大量的記錄,但要有足夠完整的(包括方案和所有結論) ,以保證制商能對驗證的充分性進行評估。
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