[外语类试卷]专业英语四级(公共健康类阅读理解)模拟试卷1及答案与解析.doc
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1、专业英语四级(公共健康类阅读理解)模拟试卷 1及答案与解析 0 The European Commission said on Thursday it would toughen the regulation of medical devices as a result of concerns raised by breast implants produced by the defunct French company PIP, even as a scientific expert review it ordered concluded there was currently “insuf
2、ficient evidence“ that women using its products faced greater health risks than others. John Dalli, health and consumer policy commissioner, pledged to examine surveillance and operation of the “notified bodies“ that scrutinise medical devices across the EU in a current review of legislation, stress
3、ing: “The capacity to detect and minimise the risk of fraud must be increased.“ His comments followed an official report released on Wednesday in France that called for national and EU-wide co-operation including random inspections and sampling of medical devices to prevent a repeat of the fraudulen
4、t use of substandard non-medical-grade silicone by PIP in implants sold to up to 400,000 women around the world. Xavier Bertrand, Frances minister of health, called for enhanced action in France and across Europe in the wake of the study, which highlighted that Afssaps, the French medical regulator,
5、 did not inspect PIP from 2001 until a tip-off led officials to inspect and close down the company in 2010. Jean-Claude Mas, its founder, is under police investigation for manslaughter. Mr. Bertrand has pledged to hire more health inspectors and undertake random checks on medical device companies fo
6、llowing growing concerns over its regulatory system highlighted by the widespread use of PIPs substandard breast implants. A French decision at the end of last year to offer all women free removal of PIP implants triggered similar proposals in the UK, Germany and the Czech Republic and has helped sp
7、ark a fresh debate over tougher EU regulation of medical devices, which are subject to far less scrutiny than pharmaceuticals. However, a review released on Thursday by the EUs own Scientific Committee on Emerging and Newly Identified Health Risks concluded: “Breast implants can fail, regardless of
8、manufacturer, and the probability of failure increases with time since implantation. In most cases, breast implant failure appears to be without identifiable health consequences for the patient with the exception of possible local complications.“ It stressed that limited data meant that while there
9、was no link between breast implants and cancer, there was a need for further work to understand the specific risks from the PIP products. Mr. Bertrand has endorsed calls for a parliamentary inquiry in France as well as a report from the countrys social affairs inspectorate, mirroring similar moves t
10、hat led to tough new requirements for the pharmaceutical industry introduced last year in the wake of concerns about Serviers drug Mediator. Medical device manufacturers have called for reforms to ensure that the national “notified bodies“ which audit the quality of their products across Europe are
11、of a consistently high standard, while cautioning that tough new regulatory requirements could harm the EUs competitive advantage. The French study showed that Afssaps had received multiple warnings over the relatively high failure rate of PIP implants compared with those made by other companies, ev
12、en though the overall proportion remained modest. From Financial Times, February 2, 2012 1 _is the manufacturer of the breast implants under scrutiny. ( A) European Commission ( B) PIP ( C) Afssaps ( D) Xavier 2 According to the passage, “notified bodies“ in Paragraph 2 are responsible for_. ( A) pr
13、oposing legislation, implementing decisions in European Union ( B) producing and marketing the medical devices across the EU ( C) providing some scientific advice to the European Commission ( D) assessing whether a product meets certain preordained standards 3 Which of the following statements is IN
14、CORRECT according to the passage? ( A) Women using the breast implants faced greater health risks. ( B) The capacity to detect the risk of fraud should be increased. ( C) An official report called for cooperation in France and in other parts of EU. ( D) Frances minister of health has pledged to hire
15、 more health inspectors. 4 Which of the following countries have not all proposed to offer women free removal of PIP implants? ( A) France, Germany, UK ( B) Germany, UK, Czech ( C) US, Germany, Czech ( D) Germany, France, Czech 5 Which of the following statements is true according to the passage? (
16、A) There is a consensus on the EU regulation of medical devices in the European Union. ( B) All breast implant failure appears to be without identifiable health consequences. ( C) Tough new regulatory requirements could harm the EUs competitive advantage. ( D) The overall proportion of the implant f
17、ailure is relatively high compared with others. 5 Health Minister Nicola Roxons latest proposal that patients be allocated to doctors on a list basis is straight out of the playbook of Britains National Health Service. Lets think about this from the patients point of view. Some doctors are better th
18、an others, the same as some plumbers are better than others. The reason may be a better bedside manner; it may be they are more competent; it may be just that there is a simple personality clashit may just be that, at times, the patient wants a second opinion. Or it might be that the patient has a p
19、otentially embarrassing problem that he or she does not want to discuss with his or her regular general practitioner. Some people who are ill-suited to their career choice are always going to slip through the system. In other words, if you are allocated a doctor you dont like or who is a dud, you ar
20、e likely to be stuck with him. Of course, the government will make some noises about “freedom of choice“; but in the end, a doctor who hangs up his shingle and succeeds or fails according to the quality of service he offers is going to provide a better quality of service than a public employee. Now,
21、 all doctors, including general practitioners, must be members of the appropriate professional body, which accredits them as qualified practitioners. This means they must first finish medical school and then qualify as surgeons, physicians, ophthalmologists or psychiatrists. This postgraduate traini
22、ng is arduous and expensive, and practitioners naturally expect a return on their investment of time, energy and moneythe average medical graduate is left with tens of thousands of dollars in university fees. Much is made of the top professionals who make millions, but the average GP is running a pr
23、actice that gives him a barely adequate return on his investment in professional development. Indeed, many GPs complain they are virtually government employees relying on Medicare to pay their bills, but the “virtually“ is important. They remain independent professionals who succeed or fail accordin
24、g to the service they provide. The recent moves to widen the scope of nurse practitioners concern many GPs. While nurse practitioners may have a role in isolated areas, a nurse is not a substitute for a general practitioner, who has years of undergraduate and postgraduate training in family medicine
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