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Category: Compliance & Regulatory

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This course covers the common purpose of regulations pertaining to human subjects research, the definition of human subject, categories exempt from human subjects regulations according to the 2017 Final Rule,...
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This course covers the common purpose of regulations pertaining to human subjects research, the definition of human subject, categories exempt from human subjects regulations according to the 2017 Final Rule, and the three fundamental principles for the protection of human subjects as described by The Belmont Report.
This course covers the common purpose of regulations pertaining to human subjects research, the definition of human subject, categories exempt from human subjects regulations according to the 2017 Final Rule, and the three fundamental principles for the protection of human subjects as described by The Belmont Report.
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Produced by: HCCS - Retail Only
This course covers the purpose of informed consent, from whom informed consent must be obtained, general requirements for informed consent and the two formats in which consent can be presented.
This course covers the purpose of informed consent, from whom informed consent must be obtained, general requirements for informed consent and the two formats in which consent can be presented.
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Produced by: HCCS - Retail Only
This course covers the term vulnerable subjects as it pertains to research, the categories of vulnerable subjects and the protections afforded them by federal regulations.
This course covers the term vulnerable subjects as it pertains to research, the categories of vulnerable subjects and the protections afforded them by federal regulations.
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Produced by: HCCS - Retail Only
This course covers the definition of a clinical trial and Investigator-sponsored research, the FDA's role in clinical trials in the United States, the phases of a clinical trial, the roles and...
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This course covers the definition of a clinical trial and Investigator-sponsored research, the FDA's role in clinical trials in the United States, the phases of a clinical trial, the roles and responsibilities of the people involved, and the difference between practice and research.
This course covers the definition of a clinical trial and Investigator-sponsored research, the FDA's role in clinical trials in the United States, the phases of a clinical trial, the roles and responsibilities of the people involved, and the difference between practice and research.
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Produced by: HCCS - Retail Only