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临床试验（clinical trial）
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听力原文： At the end of the total accounting period and after all transactions have been journalized and posted, the equality of the debit and credit entries is checked by preparing a trial balance. A trial balance is a schedule that lists the titles of the accounts in the general ledger and their debit or credit balances. If the trial balance is in balance, the financial statements can be prepared. If a trial balance does not agree, it implies that an error or errors have been made. The account balances, postings and the journal entries must be checked until the error is found. A trial balance does not prove that all transactions have been recorded or that the ledger is correct. The trial balance may still agree when a transaction is not journalized, a journal entry is not posted, an entry is posted twice, incorrect accounts are used in journalizing or posting, or offsetting errors are made in recording the amount of a transaction.24. How does the accountant check the equality of the debit and credit entries?25.What is a trial balance?26.What is implied if a trial balance does not agree?(24)A．By posting all the entries.B．By preparing a trial balance.C．By comparing the entries on both sides.D．By recording all the entries once more.
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The income statement is prepared from ().
A.the income statement columns of the work sheetB.the adjusted trial balanceC.either the adjusted trial balance or the income statement columns of the work sheetD.both the adjusted trial balance and the income statement columns of the work sheet
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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
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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?
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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
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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
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. Clinical trials provide the only hope______.A: candidates for clinical trialsB: during the trialC: medical knowledgeD: in humansE: before participationF: for some patients
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
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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
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冠心病监护病房为（）。A、intensive care unitB、coronary care unitC、acute myocardial infarctionD、Clinical common crisisE、Clinical Intensive Care
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单选题After repair, the voyage trial of the M-E should be done （）A
after the mooring trial has passedB
before the mooring trialC
under the surveyors supervisionD
after repair
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单选题According to the regulation of the voyage trial on new ship,（）is one of the trial items of the UMS ship bridge control.A
starting and direction changing trialB
cancelling accelerating function trialC
lowest stable speed trialD
continuous running trial
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单选题When carrying out mooring trial, the （） trial of the MEis not necessary.A
startingB
torsion vibrationC
direction changingD
running
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单选题When carrying out the voyage trial, the M-E is not necessary to take（）trial.A
startingB
runningC
running-inD
direction changing
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单选题Before "stand-by" is rung on the engine telegraph, it is usual to give the main engine （） ahead and astern.A
a brief trial with turning gearB
a brief trial on powerC
a long trial by steering gearD
one minutes trial with windlass
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