Abstract
This chapter deals with the fundamental principles of ethical research. Although there is particular emphasis on the process of initial ethical review of research, it is important to note that the ethical obligations of researchers continue throughout the entire continuum of the research process. The paramount importance of protecting the privacy and confidentiality of research participants is discussed. Particular emphasis is placed on the process of informed consent, and step-by-step practical guidelines are described. The issue of inclusivity in research is touched upon, and suggestions are provided. Practical advice is provided for researchers to guide their interactions with research ethics boards.
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References
Canadian Institutes of Health Research, Natural Sciences and Engineering Research Council of Canada, and Social Sciences and Humanities Research Council, Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans (2018). http://www.pre.ethics.gc.ca/eng/documents/tcps2-2018-en-interactive-final.pdf
https://www.hhs.gov/ohrp/regulations-and-policy/regulations/common-rule/index.html
http://www.cihr-irsc.gc.ca/e/documents/ethics_research_lifecycle-en.pdf
https://www.cdha.nshealth.ca/discovery-innovation/discovery-innovation/resources
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Harnett, J.D. (2021). Research Ethics for Clinical Researchers. In: Parfrey, P.S., Barrett, B.J. (eds) Clinical Epidemiology. Methods in Molecular Biology, vol 2249. Humana, New York, NY. https://doi.org/10.1007/978-1-0716-1138-8_4
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DOI: https://doi.org/10.1007/978-1-0716-1138-8_4
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Publisher Name: Humana, New York, NY
Print ISBN: 978-1-0716-1137-1
Online ISBN: 978-1-0716-1138-8
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