How does irb guidance differ from hipaa

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Reference no: EM133653296

Assignment:

Informed consent is an important topic in healthcare and clinical research. The policies and regulations that protect the public in those two scenarios are HIPAA and IRB guidelines, respectively. They are somewhat different in their purposes.

Consider this week's reading assignment - the FDA's Frequently Asked Questions (FAQ) page on Institutional Review Boards.

How does IRB guidance differ from HIPAA? Be specific. What are some key precautions that should be taken in obtaining informed consent from research participants? Does the process differ with current versus new patients in clinical research?

Reference no: EM133653296

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How does irb guidance differ from hipaa : What are some key precautions that should be taken in obtaining informed consent from research participants?

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