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单选题
Clinical Practice Guidelines代表（）
A
临床操作规程指南
B
评价研究证据
C
临床实践指南
D
病例对照研究
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考题
Three types of written media used in organizations are _____, _____, and ______.A manual, letters, guidelinesB individually-oriented, legally-oriented, organizationally orientedC guidelines, forms, proceduresD letters, guidelines, brochuresE letters, contracts, policies.
考题
34 Three types of written media used in organizations are _____, _____, and ______.A. manual, letters, guidelinesB. individually-oriented, legally-oriented, organizationally orientedC. guidelines, forms, proceduresD. letters, guidelines, brochuresE. letters, contracts, policies
考题
grammar practice is usually divided into two categories, _______________.
A. meaningful drilling and communicative drillingB. mechanical drilling and meaningful drillingC. mechanical practice and meaningful practiceD. meaningful practice and communicative practice
考题
下列关于GCP叙述错误的是A、GCP即为药物临床试验管理规范B、是指任何在人体(特指患者)进行的药品系统性研究C、目的在于保证临床试验过程的规范D、可揭示试验用药品的作用和不良反应等E、是Good Clinical Practice的简称
考题
1．I don't have a partner __________volleyball __________．A． to practice;/B． practice; withC． to practice; withD． practice;/
考题
Which of the following statements about meaningful practice in grammar teaching is NOT true?
A．Meaningful practice aims at form accuracy.
B．Meaningful practice focuses on the production and comprehension of meaning.
C．There is no clear cut between mechanical and meaningful practice.
D．Practice based on prompts is usually considered as meaningful practice.
考题
共用题干
Clinical Trials1. Many clinical trials are done to see if a new drug or device is safe and effective for people to use.Sometimes clinical trials are used to study different ways to use the standard treatments so they will be more effective,easier to use,and/or decrease side effects.Sometimes,studies are done to learn how to best use the treatment in a different population,such as children,in whom the treatment was not previously tested.2. It is important to test drugs and medical products in the people they are meant to help.It is also important to conduct research in a variety of people because different people may respond differently to treatments.Some people participate in clinical trials because they have exhausted standard treatment options .Other people participate in trials because they want to contribute to the ad-vancement of medical knowledge.3. The FDA（食品及药物管理局）works to protect participants in clinical trials and to ensure that people have reliable information as they decide whether to join a clinical trial.Although efforts are made to control the risks to clinical trial participants,some risks may be unavoidable because of the uncertainty inherent（内在的）in medical research studies involving new medical treatments.4. People should learn as much as possible about the clinical trials that interest them.They should also feel comfortable discussing their questions and concerns with members of the health care team. Prospective（预期的）participants should understand what happens during the trial ,the type of health care they will receive,and any costs to them.Anyone considering a clinical trial should also know that there are benefits and risks associated with participating. Paragraph 2______A: Are clinical trials safe?B: What are clinical trials?C: What should people know before participating in a clinical trial?D: Who should consider clinical trials and why?E: Where are clinical trials conducted?F: Why are clinical trials done?
考题
共用题干
Clinical Trials1 Many clinical trials are done to see if a new drug or device is safe and effective for people to use .Sometimes clinical trials are used to study different ways to use the standard treatments so they will be more effective,easier to use,and/or decrease side effects. Sometimes,studies are done to learn how to best use the treatment in a different group, such as children,in whom the treatment was not previously tested.2 It is important to test drugs and medical products in the people they are meant to help,It is also important to conduct research in a variety of people because different people mayrespond differently to treatments.Some people participate in clinical trials because they have exhausted standard treatment options.Other people participate in trials because they want to contribute to the advancement of medical knowledge.3 The FDA（食品及药物管理局）works to protect participants in clinical trials and to ensure that people have reliable information as they decide whether to join a clinical trial. Although efforts are made to control the risks to clinical trial participants,some risks may be unavoidable because of the uncertainty inherent（内在的）in medical research studies involving new medical treatments.4 People should learn as much as possible about the clinical trials that interest them.They should also feel comfortable discussing their questions and concerns with members of thehealth care team. Prospective（预期的）participants should understand what happens during the trial,the type of health care they will receive,and any costs to them.Anyone considering a clinical trial should also know that there are benefits and risks associated with participating. Reliable information should be available to_________.A: for some patientsB: before participationC: in humansD:medical knowledgeE: during the trialF: candidates for clinical trials
考题
共用题干
Clinical Trials1. Many clinical trials are done to see if a new drug or device is safe and effective for people to use.Sometimes clinical trials are used to study different ways to use the standard treatments so they will be more effective,easier to use,and/or decrease side effects.Sometimes,studies are done to learn how to best use the treatment in a different population,such as children,in whom the treatment was not previously tested.2. It is important to test drugs and medical products in the people they are meant to help.It is also important to conduct research in a variety of people because different people may respond differently to treatments.Some people participate in clinical trials because they have exhausted standard treatment options .Other people participate in trials because they want to contribute to the ad-vancement of medical knowledge.3. The FDA（食品及药物管理局）works to protect participants in clinical trials and to ensure that people have reliable information as they decide whether to join a clinical trial.Although efforts are made to control the risks to clinical trial participants,some risks may be unavoidable because of the uncertainty inherent（内在的）in medical research studies involving new medical treatments.4. People should learn as much as possible about the clinical trials that interest them.They should also feel comfortable discussing their questions and concerns with members of the health care team. Prospective（预期的）participants should understand what happens during the trial ,the type of health care they will receive,and any costs to them.Anyone considering a clinical trial should also know that there are benefits and risks associated with participating. Learn as much as you can about a clinical trial______.A: candidates for clinical trialsB: during the trialC: medical knowledgeD: in humansE: before participationF: for some patients
考题
共用题干
FDA : Human , Animal Waste Threatens ProduceThe biggest food safety risk for fresh fruits and vegetables as they are grown,picked or processed comes from human and animal waste,the US Food and Drug Administration(FDA)said Friday.More than 9,000 Americans die each year from food-borne diseases and some scientists believe fresh produce is the biggest carrier of contamination.The FDA issued a set of draft guidelines for US and foreign growers to carefully monitor worker hygiene, water quality,manure management and transportation.These 34-page draft guidelines urged growers to give workers lessons on basic hygiene such as using soap to wash their hands,covering wounds that could come into contact with produce,and using only clean toilets.The FDA guidelines identified"the major source of contamination"for fresh produce as human or animal feces."We think just proper controls and proper attention to detail would make a big difference in food safety,"said an FDA official."It is our belief that these guidelines would not be very costly."But grower groups disagreed with the FDA's assessment."Most food-borne disease outbreaks that happen further down the distribution line are due to contamination because people preparing food are not properly washing their hands,"said Stacey Zawal,an official with United Fresh Fruit and Vegetable Association."That is not necessarily true for growers and packers."Some US grower organizations have expressed concern that the agency is interfering with on-farm practices.Others object to the FDA's proposal to have growers formally document the picking,handling and transportation of produce so that health officials could quickly recall foods if necessary.Consumer groups criticized the FDA guidelines as of little use because they will not carry the force of law.But stricter regulations could evolve as researchers find new technology or methods to kill harmful bacteria or parasites,the FDA said.The FDA recommendations are due to be made final by the FDA later this year for use by US and foreign growers.The matter of encouraging foreign growers to adopt the guidelines remains somewhat tricky but FDA officials say it is vital because of the huge amount of imported produce.An FDA official said that putting the guidelines into practice_.A:would be too costly to be effective B:would not cost any moneyC:would not be very expensive D:would need lots of money
考题
In modern clinical practice, doctors personally assess patients in order to ______, treat, and prevent disease using clinical judgment.A.remedy
B.diagnose
C.infect
D.judge
考题
下列关于GCP叙述错误的是A.GCP即为药物临床试验管理规范
B.目的在于保证临床试验过程的规范
C.是Good Clinical Practice的简称
D.是指任何在人体(特指患者)进行的药品系统性研究
E.可揭示试验用药品的作用和不良反应等
考题
中药材种植单位必须执行（）A、GAP中药材生产质量管理规范B、GLP药物非临床研究质量管理规范C、GCP药品临床试验管理规范（Good Clinical Practice,GCP）D、GMP药品生产质量管理规范药品经营质量管理规范
考题
冠心病监护病房为（）。A、intensive care unitB、coronary care unitC、acute myocardial infarctionD、Clinical common crisisE、Clinical Intensive Care
考题
单选题Which of the following statements about meaningful practice is NOT true?A
Meaningful practice aims at form accuracy.B
Meaningful practice focuses on the production and comprehension of meaning.C
There is no clear cut between mechanical and meaningful practice.D
Practice based on prompts is usually considered as meaningful practice.
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