pharmaceutical administration 中文意思是什麼

pharmaceutical administration 解釋
藥物管理
  • pharmaceutical : adj. 1. 制藥（學）上的。2. 藥劑師的。3. 應用藥物的。n. 藥物。adv. -ly
  • administration : n 1 管理，掌管，經營；〈英國〉行政，施政。2 行政機關，局[處、署]；〈A 主美〉政府。3 給與；施行。4...
  1. So far 20000 square meters of modern pharmaceutical workshop has obtained gmp approval from the states medicine administration, and shenfeng bee products have also been designated as the unique healthcare products for the chinese women volleyball team

    建成的2萬多平米的現代藥廠已獲國家藥監局的gmp認證。神蜂系列蜂產品是中國女排指定的唯一專用保健蜂產品。
  2. The ephedrine not exported must not be disposed of without authorization and without the approval of the state department of pharmaceutical administration

    未經國家藥品管理部門批準，不得擅自處理未出口的麻黃素。
  3. Conclusion : only by integrating blood drug concentration monitoring with clinical pharmaceutical care by pharmacists can rational administration of digoxin to patients be realized

    結論：只有將地高辛血藥濃度監測與臨床藥學服務緊密結合，使地高辛給藥方案由常規化、經驗化轉向個體化，才能真正做到合理用藥。
  4. 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。
  5. 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。
  6. Suggestions on medical institute pharmaceutical administration

    對醫療機構藥事管理若干問題的意見和建議
  7. Evolution and development of the modern pharmaceutical affairs administration system in china

    我國近現代藥事管理體制的演變與發展
  8. The annual production plan of ephedrine shall be examined and finalized by the state department of pharmaceutical administration

    麻黃素的年度生產計劃由國家藥品管理部門審定。
  9. Certificates for ephedrine purchase and use shall be uniformly printed by the state department of pharmaceutical administration and one certificate shall be valid for a single use

    麻黃素購用證明由國家藥品管理部門統一印製，一證一次使用有效。
  10. Certificates for purchase and use for ephedrine export shall be uniformly printed by the state department of pharmaceutical administration and one certificate shall be valid for a single use

    麻黃素出口購用證明由國家藥品管理部門統一印製，一證一次使用有效。
  11. The designated enterprises for the production of ephedrine shall be appointed by the state department of pharmaceutical administration and submitted to the office of the national anti - drug leading group for the record

    麻黃素定點生產企業由國家藥品管理部門指定，報全國禁毒工作領導小組辦公室備案。
  12. No designated production enterprise of ephedrine shall expand the production scale of ephedrine in the form of technology transfer, joint management or establishing branch plant without the approval of the state department of pharmaceutical administration

    未經國家藥品管理部門批準，麻黃素定點生產企業不得以技術轉讓、聯營、設分廠等形式擴大麻黃素的生產規模。
  13. An ephedrine export enterprise shall go through the formalities for the obtainment of the certificate of purchase and use for ephedrine export at the state department of pharmaceutical administration along with the ephedrine export license issued by the ministry of foreign trade and economic co - operation and the afore - said materials and make the purchase at the designated ephedrine management enterprise appointed

    麻黃素出口企業持外經貿部簽發的麻黃素出口許可證及上述有關材料，到國家藥品管理部門辦理麻黃素出口購用證明，到指定的麻黃素定點經營企業購買。
  14. An application in writing shall be filed at the department of pharmaceutical administration of a province, an autonomous region or a municipality directly under the central government for the purchase of ephedrine, a certificate for purchase and use obtained upon examination and approval and the purchase made at the designated management enterprise of ephedrine appointed

    購買麻黃素應先向省、自治區、直轄市藥品管理部門提出書面申請，經審查同意后辦理購用證明，併到指定的麻黃素定點經營企業購買。
  15. Obtained the solid medical plastic bottle registration certificate that state pharmaceutical inspection administration issued in the first batch in 2001 country s powder bag word 20010082, obtain liquid medical plastic bottle registration certificate 2002 word 20020024, powder bag of country,

    年首批取得國家藥品監督管理局頒發的固體藥用塑料瓶注冊證國藥包字，年取得液體藥用塑料瓶注冊證國藥包字。
  16. " the cooperation between town health and our center will benefit town health to leverage on the mainland s professional experience, resources and huge market in chinese medicine in the research and development of pharmaceutical and healthcare products for the china market. in addition, our center will play a supporting role in assisting town health to develop its new products and effectively enhancing its capability for future development. " commented mr yu wen ming, director, national center for traditional chinese medicine, state administration of traditional chinese medicine, p. r. c

    中國中醫藥科技開發交流中心於文明稱：康健國際控股有限公司與中國中醫藥科技中心的合作，有利於康健運用國內中醫藥專家、中藥資源及大市場優勢，研發出適合中國市場的醫藥保健產品，同時中國中醫藥科技中心會在新藥研發項目上成為康健的後援，並有效地支持康健的發展。
  17. Congress has tacked on to the normal 20 - year patent term ( which until 1995 was only 17 years ) an additional term of up to 5 years for the time it takes a pharmaceutical manufacturer to get a new drug approved by the food and drug administration

    國會已經為專利所有權在原有的20年的期限（ 1995年以前僅為17年）的基礎上為制藥廠商為新藥取得食物以及藥品管理局的批準額外提供了5年的期限。
  18. Headquartered in beijing, national center for tcm operates under the state administration of traditional chinese medicine with the mission to promote, and develop chinese pharmaceutical and healthcare related products and technological advancement

    主要業務包括協助國家中醫藥管理局中醫藥科技成果推廣計劃、重大科技開發項目，開發及推廣新藥、中西醫藥新產品，舉辦交流及展銷活動，開拓中醫藥技術市場及有關之培訓等等。
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