藥物注冊 的英文怎麼說

中文拼音 [yàowùzhùcè]
藥物注冊 英文
drug legislation
  • 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...
  • 物 : 名詞1 （東西） thing; matter; object 2 （指自己以外的人或與己相對的環境） other people; the outsi...
  • 注 : Ⅰ動詞1 （灌入） pour; irrigate 2 （集中） concentrate on; fix on; focus on 3 （用文字來解釋字句）...
  • 冊 : Ⅰ名詞（冊子） volume; book Ⅱ量詞copy
  • 藥物 : medicinal; medicine; medicant; medication; drug; pharmaceuticals; medicaments
  • 注冊 : logon; post; charge of registration; register
  1. General out - patient clinic by hospital authority

    搜尋注冊藥物（只提供英文版本）
  2. Authorised dispensaries medicines

    注冊藥房（藥物）
  3. Chinese moa animal medicine and instrument of husbandry and veterinary bureau in charge of licensure of animal medicine product

    美國、歐盟、中國對獸用生物製品、獸用藥品產品注冊申報材料的具體要求也有所不同。
  4. Administration of veterinary biologic and animal drug in the united states of america is belongs to two agency : aphis - cvb and fda - cvm. mostly the legal basis for product licensure include : vst acts, 9cfr, vsm, federal food, drug, and cosmetic act, 21cfr etc. the european medicines evaluation agency for product used in animal is emea - cvmp. the legal basis on three director ( 81 / 851 / eec, 81 / 852 / eec, 2001 / 82 / eec ) and one regulation ( 2309 / 93 / eec )

    美國獸用生物製品和獸用藥品歸兩個部門管理，獸用生物製品由美國農業部動植物檢疫局（ aphis ）下屬的獸醫生物製品中心（ cvb ）負責，獸用藥品由美國健康和人類服務部食品與藥物管理局（ fda ）下屬的獸醫藥品中心（ cvm ）負責；產品注冊的有關法律法規主要包括生物製品的《病毒-血清-毒素法》 （ vstacts ） 、 《聯邦法規9 》 （ 9cfr ）及一些規章如美國獸醫局發布的《美國農業部獸醫服務局規章》 （ vsm ）等，獸用藥品的《聯邦食品、藥品與化妝品法》和《聯邦法規21 》等。
  5. Prophylaxis should be prescribed by registered doctors

    預防流感藥物，應由注冊醫生處方。
  6. We studied situation of the international botanical drug ' s registration and quality control, summarized three main modes of the quality control and analyze the difference and homology of the two control system represented by the europe - usa & japan separately. the development of botanical drug ' s quality control is also discussed in our study

    本課題研究了國際植物藥注冊和質量控制現狀，總結出植物藥質量控制的三種主要模式，並分析了以歐美為首的化學成分控制模式和日本為首的標準湯劑控制模式的相同點和不同點，探討了植物藥質量控制的發展趨勢。
  7. The sequence of quinolone resistant determing regions ( qrdr ) of gyrase subuint a of salmonella analysis indicated that the gyra gene of strain sll - 3 share 95. 8 % respectively identities with the sequence that griggs reported which showed a high homology between the strains

    對1株耐藥菌株的染色體pcr擴增產物進行了測序，與griggs等在genbank中注冊的沙門氏菌gyra基因qrdr的編碼序列進行比較，同源率為95 . 8 。
  8. Application for registration as an importer exporter of pharmaceutical products

    藥品/藥劑製品/物質注冊申請書
  9. Dr tsang said the government would follow scezd recommendations and the public medical sector would use the antiviral stockpile to provide treatment to infected patients in the event of pandemic influenza. he reminded that the dispensing of antiviral drugs for influenza ( tamiflu and relenza ) requires prescriptions from registered medical practitioners

    曾醫生表示政府將遵照新發現及動物傳染病科學委員會的建議，在大流感出現時，公營醫院將使用抗流感病毒藥物醫治受感染的病人，他提醒業界要有注冊醫生的處方，才可出售抗流感病毒藥物（特敏福及樂感清） 。
  10. Class 5 pharmaceutical and veterinary preparations ; sanitary preparations for medical purposes ; dietetic substances adapted for medical use, food for babies ; plasters, materials for dressings ; material forstopping teeth, dental wax ; disinfectants ; preparations for destroying vermin ; fungicides, herbicides

    商標注冊類別5醫用和獸醫用制劑，醫用衛生制劑，醫用營養品，嬰兒食品，膏藥，繃敷材料，填塞牙孔和牙模用料，消毒劑，消滅有害動物制劑，殺真菌劑，除莠劑。
  11. Dar controlling to ensure all outgoing goods with proper documents

    確保每一訂單貨物配送相應的進口藥品檢驗報告書和進口藥品注冊證。
  12. Oseltamivir can be taken for prevention of flu but it should be prescribed by registered doctors

    奧斯他韋作為一種預防流感藥物，應由注冊醫生處方，市民
  13. Once a medicine is approved for registration, a registration number is issued

    為已經注冊的藥物加上標簽藥物一經核準注冊，可獲發出一個注冊編號。
  14. Published by the department of health. it contains information on the product names, active ingredients and the registration number of the medicines

    載有關于香港注冊藥物的資料，是有用的參考依據，這本目錄列載藥劑製品的名稱、有效成分及注冊編號。
  15. You can search online for registered pharmaceuticals in hong kong by registration number, product drug name, active ingredient or certificate holder

    你可根據注冊編號、產品藥物名稱、主要成分或證書持有人，於此網站搜尋已在香港注冊的藥物（只提供英文版本） 。
  16. At present, there are about 800 pharmaceutical products registered in hong kong as containing alkaloids of ephedra, most of which are indicated for the relief of common cold, nasal congestion, chronic rhinitis and hay fever

    現時，約有八百種在香港注冊的藥劑製品含有麻黃生物鹼，大部分註明可用於減輕一般傷風、鼻塞、慢性鼻炎及花粉熱的癥狀。
  17. In addition to this requirement on pre - market registration, pharmaceutical products containing alkaloids of ephedra, being part i poisons, can only be sold by authorised sellers of poisons under the supervision of a pharmacist

    除根據規定必須在銷售前獲得注冊外，含有麻黃生物鹼的藥劑製品被列為第i部毒藥，只可在藥劑師在場監督的情況下，由獲授權毒藥銷售商出售。
  18. The dh has no record of this product having been imported into hong kong for sale, or having been submitted for registration

    ?生署沒有此產品入口香港作出售用途的記錄，亦沒有其申請藥物注冊的記錄。
  19. The dh has no record of these products having been imported into hong kong for sale, or having been submitted for registration

    ?生署沒有此產品入口香港作出售用途的記錄，亦沒有其申請藥物注冊的記錄。
  20. The requirements of dossier contents for licensing application are different in u. s. a, eu and china. this dissertation explains the dossier detailedly include : the dossier requirements of veterinary domestic, import product and animal drug product in u. s. a. the dossier requirements of immunological medical product, medicine product and unimmunological medical product in eu. and chinese dossier requirement of domestic new veterinary biological and drug product, import eterinary biological and drug product

    本文詳細介紹了美國獸用生物製品中國內產品和進口產品的注冊申報材料及獸用藥品的材料要求；介紹了歐盟對免疫用獸醫藥品和獸醫藥品、非免疫用獸醫藥品的書寫格式和內容的要求；同時詳細說明了中國對申報國內新獸用生物製品和新獸藥、進口獸用生物製品和獸藥的注冊申報材料的項目要求。
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