QALaw › As part of the consent process, the federal regulations require researchers to:
Q

As part of the consent process, the federal regulations require researchers to:

1. Provide a list of the IRB members who reviewed the protocol.

2. Describe penalties that may be imposed for non-participation.

3. Provide potential subjects with information at the appropriate reading comprehension level.

4. Recommend that potential subjects discuss their decision to participate with family members.

A

Answer: 3. Provide potential subjects with information at the appropriate reading comprehension level.

Informed consent is the process of educating a patient on a research procedure that is being tested on live subjects as an alternative medical procedure. When making such a call, healthcare personnel are required that patients from 18years and above understand the terms, policies, and conditions of the procedure being tested before they sign. Informed consent is a doctrine that ensures that patients are well-educated about practices and procedures that are to be performed on them. Informed consent is to be administered for research procedures, drugs, and surgery.

3 years ago
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