药品

Acceptance criteria means the product specifications and acceptance/rejection criteria, such as acceptable quality level and unacceptable quality level, with an associated sampling plan, that are necessary for making a decision to accept or reject a lot or batch (or any other convenient subgroups of manufactured units).

验收标准指建立在相应的取样方法基础之上的、药品的质量检验标准和接受/拒收的标准(例如可接受/不可接受的质量水平)，是决定批准或拒收一批药品的必需因素。

We are also helping fund a project for "GMP" which is a more palatable form of protein in the form of food - in addition to the medical formulas available and may be able to be used as supplements to the medical formula in the coming years.

同时我们正在资助一个有GMP认证的药品研发项目，这种药品是以食物形式存在的更为美味可口的蛋白质补充品，作为目前已有的各种医疗配方奶粉的补充。

More attentions were paid to the safety and regulations of the medicine's usage in the hospitals. The Automated Drug Dispensing Machine is set to secure the medicines handlings.

医院药品使用过程的安全性和科学管理越来越受到关注，自动单剂量药品分包机的作用就是保障医院内药品使用的安全性和规范化。

Manufacture of sterile medicinal products, use of ionising radiation in the manufacture of medicinal products, manufacture of biological medicinal products and computerized systems.

除另有规定外，GMP的基本条款适用于人血液或血浆制品。还有一些附件也适用，如无菌药品的生产，药品生产中电离辐射的使用，生物药品的生产和系统计算机化。

Fig.5 mp53 mRNA in situ hybridization signal in human HXO-Rb44 cells(Fig.a, experimental group,EG;Fig.b, control group,CG).The signal as violet-colored fine granules localized in the cytoplasm,EG weaker than CG,×1 000;Fig.c, mp53 mRNA dot blot signal,EG weaker than CG

图6～8 人HXO-Rb44药品细胞 p16、p21WAF1及Rb 免疫调查组织化学反应性，a为实验组，b为对照组，免疫调查反应细颗粒位于药品细胞核和药品细胞质，EG强于CG，×1 000；c为Rb、p21WAF1及p16蛋白斑点印迹免疫调查反应性，EG强于CG。

Objective:Analyze the purchase model of ABC classification management,stocking drugs rationally and making use of drugs efficiently.

目的：探讨药品库存ABC分类管理的采购模式，合理控制药品库存量，提高药品使用率。

The Committee for Herbal Medicinal Products shall take over the tasks of the Committee for Human Medicinal Products with regard to authorisations or registrations by Member States of herbal medicinal products.

草药品委员会应承担人用药品委员会在成员国植物药品许可和注册方面的工作。

Routine method,medium diluting method,centrifuging and centrifuging medium diluting method were for the verification of methodology on five traditional chinese medicine.

随着药品剂型的日益发展和药品标准的不断提高，及时有效地进行药品微生物限度检查是摆在药检工作人员面前的重大课题。

Shandong C.P.Freda Pharmaceutical Co., Ltd, founded in 1992, is a joint venture by C.P. Healthcare Group of Thailand, Freda International Inc. of America and Shandong Biochemical Pharmaceutical Co. of China. The company is dedicated to the development, manufacture and sale of biotechnological products and biochemical medicines.

山东正大福瑞达制药有限公司成立于1992年，由泰国正大制药集团、美国福瑞达国际有限公司和中国山东省生化药品公司共同投资，致力于生物技术产品和生化药品的研究、生产和销售，已形成眼科、皮肤科、外科及内科药品系列的研制和生产能力。

Shandong C.P.Freda Pharmaceutical Co., Ltd, founded in 1992, is a joint venture by C.P. Healthcare Group of Thailand, Freda International Inc. of America and Shandong Biochemical Pharmaceutical Co. of China. The company is dedicated to the development, manufacture and sale of biotechnological products and biochemical medicines.

公司简介：山东正大福瑞达制药有限公司成立于1992年，由泰国正大制药集团、美国福瑞达国际有限公司和中国山东省生化药品公司共同投资，致力于生物技术产品和生化药品的研究、生产和销售，已形成眼科、皮肤科、外科及内科药品系列的研制和生产能力。

And Pharaoh spoke to Joseph, saying, Your father and your brothers have come to you.

47：5 法老对约瑟说，你父亲和你弟兄们到你这里来了。

Additionally, the approximate flattening of surface strip using lines linking midpoints on perpendicular lines between geodesic curves and the unconditional extreme value method are discussed.

提出了用测地线方程、曲面上两点间短程线来计算膜结构曲面测地线的方法，同时，采用测地线间垂线的中点连线和用无约束极值法进行空间条状曲面近似展开的分析。