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- To be told that the study involves research.
- To be told any reasonably foreseeable risks, side effects or discomforts
that might be expected.
- To be told of any benefits to the participant that can be reasonably
expected.
- To be told what procedures will be administered and whether any
of them are experimental.
- To be told of appropriate alternative drugs or procedures that
might be advantageous to the participant.
- To be allowed to ask any questions about the research study before
giving consent and at any time during the course of the research study.
- To be told who they can contact with questions about the study,
their rights as a participant and who to contact in the case of a
research-related injury.
- To be allowed ample time, without pressure, to decide whether to
consent or not to consent to participate.
- To refuse to participate, for any reason, before and after the
research study has started.
- To receive a signed and dated copy of the informed consent form.
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