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Bioethical Approach for Nursing Research -Focused on the Use of Research Ethics Committees

Jeong IS

PURPOSE: This paper was written to introduce methods of using the research ethics committee (RES) from requesting the initial review to reporting the close-out for nursing researchers. METHODS: General ethical principles...
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Mission and Operation of Institutional Review Board

Kim YJ

  • KMID: 2320016
  • Yeungnam Univ J Med.
  • 2013 Dec;30(2):73-78.
An institutional review board (IRB) should independently safeguard the right, safety, and well-being of all clinical trial subjects. It should consist of members who are qualified and experienced to review...
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Current Status of the Institutional Review Boards in Korea: Constitution, Operation, and Policy for Protection of Human Research Participants

Kim OJ, Park BJ, Sohn DR, Lee SM, Shin SG

The institutional review board is crucial to ensure the scientific and ethical quality of human participant research. This paper analyzes a survey on the current constitution and operation of institutional...
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Clinical trials and ethics

Lim I, Rha SY

Based on recently developed biotechnology, many new drugs have been developed for improving patient treatment outcomes. To develop novel drugs, proper clinical trials are essential. As clinical trials involve humans...
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Ethical Considerations in Hospice and Palliative Care Research

Youn G

Along with the advances in medical technology and the economic development, more terminally ill patients are receiving hospice and palliative care services. Moreover, hospice and palliative care clinicians have been...
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Ethical and Regulatory Problems of Molecular Imaging

Jeong JM

  • KMID: 2078805
  • Korean J Nucl Med.
  • 2004 Apr;38(2):140-142.
As a molecular imaging is the most up-to-date technology in Nuclear Medicine, it has complicate ethical and regulatory problems. For animal experiment, we have to follow institutional animal care committee....
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Need for Clinical Trial Registry and Institutional Review Board Approval in Human Subjects Research

Kim SY

No abstract available.
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Institutional review board (IRB) and ethical issues in clinical research

Kim WO

Clinical research has expanded tremendously in the past few decades and consequently there has been growing interest in the ethical guidelines that are being followed for the protection of human...
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Management and Ethics of Biobank; Biorepository

Shin BK, Choi JW, Lee H, Kim A, Kim I, Kim HK

  • KMID: 2073750
  • Korean J Pathol.
  • 2005 Dec;39(6):372-378.
Research access to a large number of high-quality biospecimen, adequately annotated and ethically acquired, is critical to an improved understanding of disease and ultimately new development of effective diagnostic markers...
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Protection of Personal Information in Medical Journal Publications

Huh S

It aimed to present the definition of personal information based on Korean laws that protect personal information and the process of protection of personal information in journal publishing based on...
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Bioethics and Protection of Personal Information in Experimental Studies

Kim OJ

  • KMID: 2303868
  • Korean J Epidemiol.
  • 2007 Jun;29(1):1-12.
Experimental studies involve intervention and manipulation of study elements such as randomization of the participating groups. In general, experimental studies involving human are riskier than observational studies, demanding robust ethical...
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The Suggestions for Improving the Institutional Review Board (IRB) in Clinical Trials: Focusing on Continuing Management

Shin HY

  • KMID: 2334464
  • J Korean Soc Clin Pharmacol Ther.
  • 2011 Jun;19(1):5-13.
As Korea has increasing number of clinical trials in recent years, institutional review boards (IRBs) are facing new challenges. The IRB should review submitted documents and supervise clinical trials from...
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Institutional Review Boards and Bioethical Issues for Otologists and Audiologists

Park MK, Lee BD

Otologists and audiologists care for patients and conduct clinical research to find more effective treatments that benefit patients. Institutional Review Board (IRB) permission is necessary for conducting clinical trials on...
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Survey of Institutional Review Board Approval and Informed Consent in Clinical Research of Korean Anesthetic Society

Koh W, Sim J, Ahn W

BACKGOUND: All medical research requires approval of the institutional review board ( IRB ) and informed consent from the research participants in advance. But there are reports of low rates...
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Effect of Bioethics and Safety Act in medical research

Park HW

The ethics of medical research is an important area of physician ethics. Physicians are called to respect the life, health, and personality of human subjects. In contrast to other ethical...
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Stages of Institutional Review Board Activities

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No abstract available.
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Characteristics Desired in Clinical Data Warehouse for Biomedical Research

Shin SY, Kim WS, Lee JH

OBJECTIVES: Due to the unique characteristics of clinical data, clinical data warehouses (CDWs) have not been successful so far. Specifically, the use of CDWs for biomedical research has been relatively...
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The Status of Pathology Specimen Bank in Other Countries

Bae HI, Yoon GS

  • KMID: 2073751
  • Korean J Pathol.
  • 2005 Dec;39(6):379-383.
Pathology specimen has been collected for purposes of education and research, particularly with respect to basic, developmental and translational studies in many areas of cancer research including molecular biology, immunology,...
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Let Archived Paraffin Blocks Be Utilized for Research with Waiver of Informed Consent

Kim YJ, Park JS, Ko K, Jeong CR

Advances in biomedical and genetic research have contributed to more effective public health improvement via bench-to-bed research and the emergence of personalized medicine. This has certainly showcased the importance of...
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Human Studies on Functional Foods: How They Are Regulated

Kim J, Kim JY, Won HS, Kwon HJ, Kwon HY, Jeong HI, Kwon O

Along with the steady growth of health functional food (HFF) markets, research evaluating the human effects of HFF has been expanding. In this study, we investigated the regulatory and management...
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