quality pharmaceuticals 中文意思是什麼

quality pharmaceuticals 解釋
藥物質量
  • quality : n 1 質，質量；性質，特質；品質，品位。2 優質，美質，優點。3 才能，能力，技能，素養。4 品種。5 身...
  • pharmaceuticals : 藥物學：[化學，公司][麻醉藥商店，避孕方法
  1. Article 28 rules for storage of pharmaceuticals shall be formulated and implemented by medical organizations, which must adopt necessary measures to facilitate cold storage and protection against cold, moisture, insects and rodents to ensure the quality of pharmaceuticals

    第二十八條醫療機構必須制定和執行藥品保管制度，採取必要的冷藏、防凍、防潮、防蟲、防鼠等措施，保證藥品質量。
  2. Article 65 according to the needs of supervision and inspection, pharmaceutical supervisory and administrative departments may conduct sampling examinations on the quality of pharmaceuticals

    第六十五條藥品監督管理部門根據監督檢查的需要，可以對藥品質量進行抽查檢驗。
  3. Article 66 the pharmaceutical supervisory and administrative departments under the state council and of the provinces, autonomous regions and municipalities directly under the central government shall regularly promulgate the results of sampling examinations and inspections on the quality of pharmaceuticals, and shall, in the case of improperly published statements, amend such statements in the original published documents

    第六十六條國務院和省、自治區、直轄市人民政府的藥品監督管理部門應當定期公告藥品質量抽查檢驗的結果；公告不當的，必須在原公告范圍內予以更正。
  4. 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。
  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藥品生產企業的深入調研，研究了藥品生產物流過程質量管理方法，其中重點對信息集成和混批混料風險分析兩個方面進行了深入研究： 1
  6. We are a professional translation company, relate to scopes include : accountant, mechanics, electronics, chemical, bio - pharmaceuticals, motorcar and other fields, have experience in translation, handle with more than 20 kinds of different languages, such as : english, french, german, russian, arabic, danish, dutch, portuguese, japanese, turkish, spanish, italian, korea, polish, finnish, czech, norwegian, swedish, vietnamese ， greece ， hungarian ； have experts on proofread and layout co - workers, competitive price, high quality and consummate service

    我公司是專業從事翻譯服務的機構，涉及的領域包括：會計、機械、工程、電子、化工、生物制藥、汽車等方面，具有豐富的翻譯經驗，現已做過的語種有二十種：英、法、德、俄、阿拉伯、丹麥、荷蘭、葡語、日語、土耳其、西班牙、義大利、韓語、波蘭語、芬蘭語、捷克語、挪威語、瑞典語、越南語、希臘語、匈牙種語；有專業的校對和排版人員，低廉的價格和好的質量及優質的服務
  7. Article 53 packaging must meet the specific quality requirements of the pharmaceuticals and facilitate their storage, transportation and medical use

    第五十三條藥品包裝必須適合藥品質量的要求，方便儲存、運輸和醫療使用。
  8. Article 76 the person - in - charge or personnel directly liable in the enterprise or other unit which produces and sells fake medicines or produces and sells pharmaceuticals of inferior quality shall not be permitted to engage in the production and trade of pharmaceuticals for ten years, if the circumstances are serious

    第七十六條從事生產、銷售假藥及生產、銷售劣藥情節嚴重的企業或者其他單位，其直接負責的主管人員和其他直接責任人員十年內不得從事藥品生產、經營活動。
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