PART C
Directions: You will hear three dialogues or monologues. Before listening to each one, you will have 5 seconds to read each of the questions which accompany it. While listening, answer each question by choosing A, B, C or D. After listening, you will have 10 seconds to check your answer to each question. You will hear each piece ONLY ONCE.
听力原文: George Daniels lives in London. He is a watchmaker. His work continues the tradition of the English watchmakers of the 18th and 19th centuries. Today that tradition is almost dead. Daniels is the only man in the world who designs his own watches, makes all the parts himself, and then puts them together.
A Daniels' watch is the product of his hands alone. One of his watches, which is now in an American museum, took 3,500 hours to complete. He usually makes one watch a year. Each one is written "Daniels', London", and costs about 10,000 pounds. Of course, they are not ordinary watches -- they are very beautiful and will last at least three centuries.
Clocks and watches have always fascinated George Daniels. When he was five, he used to take his father's clock to pieces, and put it back together again. At school he used to repair the teachers' watches. When he was in the army, he repaired watches in his spare time. After he had left the army, he became a professional watch-repairer. Then from 1958 to 1968, he restored antique watches, and finally began making his own watches.
He is now internationally famous and many people would like him to make watches for them. Most of them will be disappointed. He chooses his customers very carefully indeed. "It must be someone who understands the subject," he says. "Not someone who'll leave the watch in the drawer only to show it to dinner guests."
What do you know about George Daniels?
A.He is one of the few remaining watchmakers in the world.
B.He is the last of the great watchmakers.
C.He is training young watchmakers.
D.He thinks watchmaking will continue for another three centuries.
第1题
A.监督检查
B.药品委托生产的委托方
C.药品委托生产的受托方
D.药品委托生产批件
E.药品生产监督管理
依法对药品生产过程进行的审查、许可认证、检查的监督管理活动是
第2题
A.监督检查
B.药品委托生产的委托方
C.药品委托生产的受托方
D.药品委托生产批件
E.药品生产监督管理
依法对药品生产过程进行的审查、许可认证、检查的监督管理活动是
第3题
A.药品委托生产的受托方
B.药品委托生产的委托方
C.药品委托生产批件
D.生产地址
E.委托生产合同
第4题
请根据以下内容回答 41~44 题
A.药品委托生产的委托方
B.药品委托生产的受托方
C.监督检查
D.药品委托生产批件
E.《药品生产许可证》
第 41 题 《药品生产许可证》换发或年检实施的现场检查,药品gmp跟踪检查,日常监督检查是()
第5题
A.药品委托生产的受托方
B.药品委托生产的委托方
C.药品委托生产批件
D.生产地址
E.委托生产合同
应提供委托生产药品的技术和质量文件,对生产全过程进行指导和监督的是
第6题
A.药品委托生产的委托方
B.药品委托生产的受托方
C.药品委托生产批件
D.生产范围和许可证编号
E.年检情况
负责委托生产药品的质量和销售的是
第7题
A.药品委托生产的委托方
B.药品委托生产的受托方
C.药品委托生产批件
D.生产范围和许可证编号
E.年检情况
负责委托生产药品的质量和销售的是
第9题
A.委托方和受托方不在同一省的,委托方所在地省级药品监督管理部门应当及时将委托生产申请的批准、变更和注销情况告知受托方所在地省级药品监督管理部门
B.委托生产双方的《药品生产许可证》、《药品生产质量管理规范》认证证书或委托生产药品批准证明文件有效期届满未延续的,《药品委托生产批件》自行废止
C.对委托方和受托方的监督检查每年至少进行一次
D.经设区的市级药品监督管理部门批准,药品生产企业可以接受委托生产药品
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