CNE/CME questions

May 2009
Clinical Trials Administrator;May2009, Vol. 7 Issue 5, p60
A quiz about articles dealing with clinical trials published within this issue is presented.


Related Articles

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  • What You Need to Know Before Becoming A Human Subject in a Clinical Trial.  // Health Letter;Mar2013, Vol. 29 Issue 3, p1 

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  • eClinical news.  // Applied Clinical Trials;Sep2010, Vol. 19 Issue 9, p8 

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  • Controlled trials: The 1948 watershed. Doll, Richard // BMJ: British Medical Journal (International Edition);10/31/98, Vol. 317 Issue 7167, p1217 

    Looks at the introduction of clinical trials method in 1948 which has played a major part in the progress of clinical medicine in the last half century. Use of concurrent controls; Introduction of randomization; Ethical considerations.

  • Auditing Clinical Data. Pyle, H. Ruth // Applied Clinical Trials;May2000, Vol. 9 Issue 5, p65 

    Explains how to conduct clinical data audits. Performance of study-oriented and investigator-oriented inspections; Use of a clinical quality assurance program to coordinate monitoring efforts; Employment of a contract research organization or site management organization; Benefits of clinical...

  • Documenting Monitoring Activities. Bohaychuk, Wendy; Ball, Graham // Applied Clinical Trials;May2000, Vol. 9 Issue 5, p72 

    Discusses steps for documenting monitoring activities during clinical trials. Monitoring visit reports; Checklist for preparation of source data verification plans; Documentation of source data verification; Case report form review at study site.

  • Q&A.  // Applied Clinical Trials;May2000, Vol. 9 Issue 5, p86 

    Presents a question-and-answer advisory on clinical trial administration. Duties of investigators; Office for Protection From Research Risks documents; Trade associations for clinical research professionals.

  • Patients' perceptions of information provided in clinical trials. Ferguson, P. R. // Journal of Medical Ethics;Feb2002, Vol. 28 Issue 1, p45 

    Background: According to the Declaration of Helsinki, patients who take part in a clinical trial must be adequately informed about the trial's aims, methods, expected benefits, and potential risks. The declaration does not, however, elaborate on what "adequately informed" might amount to, in...


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