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    Assignment No. 002 STS

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    Steffie Anne Gavina
    The document contains a 10 question multiple choice assignment about clinical trials, research ethics, and the roles of various organizations in research oversight. The questions cover topics like which government agency approves clinical trials (FDA), what phase of drug development tests safety and effectiveness in animal models, what type of consent is required from human subjects (informed consent), and examples that illustrated the need for research ethics guidelines like the Tuskegee Study.

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    Assignment No. 002 STS

    Uploaded by

    Steffie Anne Gavina
    383 views2 pages
    The document contains a 10 question multiple choice assignment about clinical trials, research ethics, and the roles of various organizations in research oversight. The questions cover topics like which government agency approves clinical trials (FDA), what phase of drug development tests safety and effectiveness in animal models, what type of consent is required from human subjects (informed consent), and examples that illustrated the need for research ethics guidelines like the Tuskegee Study.

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    The document contains a 10 question multiple choice assignment about clinical trials, research ethics, and the roles of various organizations in research oversight. The questions cover topics like which government agency approves clinical trials (FDA), what phase of drug development tests safety and effectiveness in animal models, what type of consent is required from human subjects (informed consent), and examples that illustrated the need for research ethics guidelines like the Tuskegee Study.

    Copyright:

    © All Rights Reserved
    Download as DOCX, PDF, TXT or read online from Scribd
    Download as docx, pdf, or txt
    383 views2 pages

    Assignment No. 002 STS

    Uploaded by

    Steffie Anne Gavina
    The document contains a 10 question multiple choice assignment about clinical trials, research ethics, and the roles of various organizations in research oversight. The questions cover topics like which government agency approves clinical trials (FDA), what phase of drug development tests safety and effectiveness in animal models, what type of consent is required from human subjects (informed consent), and examples that illustrated the need for research ethics guidelines like the Tuskegee Study.

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    GE6116 - Science, Technology, and Society

    ASSIGNMENT NO. 002


    1.) Part of the government in United States that gives approval to clinical trials with successful outcomes.
    Select one:
    a. Animal Models
    b. Food and Drug Administration
    c. Office for Human Research Protection
    d. Clinical Trial

    2.) It is where the effectiveness and toxicity of the drug under the development stage are tested
    Select one:
    a. Animal Models
    b. Office for Human Resource Protection
    c. Clinical Trial
    d. Informed Consent

    3.) It is what IRB requires researchers to obtain from human subjects.


    Select one:
    a. Informed Consent
    b. Office for Human Research Protection
    c. Clinical Trial
    d. Animal Models

    4.) A research which demonstrates ethical misconduct and therefore shows the need for ethical and legal
    guidelines in using humans for biomedical research.
    Select one:
    a. In Vitro
    b. Drug
    c. Tuskegee Study
    d. Gene Therapy

    5.) Prior to preclinical trials, the drugs under investigation are tested in what condition.
    Select one:
    a. In Vitro
    b. Side Effects
    c. Gene Therapy
    d. Drug

    6.) It is a substance where the use of human subjects in biomedical research is essential in its development
    and for it to be used for new therapy.
    Select one:
    a. Side Effects
    b. Drug
    c. In Vitro
    d. Gene Therapy

    7.) It's a study involving an 18-year-old male illustrates the need to disclose to the participants all risks
    involved in a biomedical research study.
    Select one:
    a. In Vitro
    b. Gene Therapy
    c. Side Effects
    d. Drug

    Assignment No. 002 P a g e |


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    GE6116 - Science, Technology, and Society

    8.) It is the institute or office where all IRBs should be registered.


    Select one:
    a. Animal Models
    b. Informed Consent
    c. Clinical Trial
    d. Office for Human Research Protection

    9.) It is a process where new drugs are tested for effectiveness and safety using human subjects.
    Select one:
    a. Food and Drug Administration
    b. Clinical Trial
    c. Office for Human Research Protection
    d. Animal Models

    10.) Aside from metabolism the initial phase of clinical testing using human subjects also determines
    what of the drug regimen?
    Select one:
    a. In Vitro
    b. Drug
    c. Gene Therapy
    d. Side Effects

    Assignment No. 002 P a g e |


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