毒物注冊 的英文怎麼說

中文拼音 [dúwùzhùcè]
毒物注冊 英文
poison registration
  • 毒 : Ⅰ名詞1 （對生物體有害的性質或物質; 毒物） poison; toxin 2 （毒品） drug; narcotics 3 （姓氏） a s...
  • 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
  • 毒物 : toxic; toxicant; poison; poisonous substance
  • 注冊 : logon; post; charge of registration; register
  1. 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。
  2. 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） 。
  3. 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。
  4. 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。
  5. For the protection of public health, any product containing ephedra or alkaloids of ephedra which is not regulated under the cmo is required to be registered with the pharmacy and poisons board ( a statutory body established under the ppo ) before it can be manufactured or sold in hong kong

    為保障公眾健康，含有麻黃或麻黃生物鹼而不受《中醫藥條例》規管的產品，必須先獲得藥劑業及毒藥管理局注冊，方可在香港製造或銷售，該管理局是根據《藥劑業及毒藥條例》成立的法定機構。
  6. In hong kong, medicines are required to be registered under the pharmacy and poisons ordinance cap 138. the purpose is to ensure that medicines available for sale are safe, effective and of good quality. this is necessary for the protection of the health of members of the general public

    根據香港法例第138章《藥劑業及毒藥條例》的規定，香港境內銷售的藥物必須注冊，藉以確保藥物安全、有效及品質優良，這項規定是保障市民健康必需的措施。
  7. Specifically, the pharmacy and poisons board proposes to add " teriparatide and its salts " to part i of the poisons list, and the first and third schedules to the pharmacy and poisons regulations so that pharmaceutical products containing such substances must be sold in pharmacies under the supervision of registered pharmacists and in their presence, with the support of prescriptions

    具體而言，藥劑業及毒藥管理局建議，加列特立帕? ；其鹽類于毒藥表的第一部及《藥劑業及毒藥規例》的附表一和附表三內，規定含有這些物質的藥劑製品必須根據處方，在注冊藥劑師在場監督下，由藥房出售。
  8. They were registered in hong kong in november 2000 and june 2001 respectively. both avandia and actos had been subject to two - year carcinogenicity studies on rodents and subsequent clinical trials on humans before their registration applications were tendered to the ppb for consideration

    有關公司為這兩種藥物向藥劑業及毒藥管理局提出申請注冊前，已就這兩種藥物在老鼠身上進行為期兩年的致癌性研究，其後也在人體進行臨?測試。
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