![]() Privacy and confidentiality of the subjects is to be maintained throughout the research process. Privacy & Confidentiality (HRPP Operations Manual, Part 3, section III, C.6.g) You should receive a signed and dated copy of the informed consent form. You are allowed to ask any questions about the study before giving consent and at any time during the course of the study. You must be allowed ample time, without pressure, to decide whether to consent (agree) to participate or not in the study. Contact information for the IRB, if you have any concerns.The risks to the your privacy and confidentiality. ![]()
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