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INFORMED CONSENT IN RESEARCH: PRACTICAL ASPECTS Souk Sen MD, MS, MPH, FHA Professor and Chair, USC Department of NeurologyHISTORY 1847 AMA's first Code of Ethics urged patients to obey their physicians

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What is informed consent in research?

Informed consent in research is the process where participants voluntarily confirm their willingness to participate in a particular study after being informed about all aspects of the research.

Who is required to file informed consent in research?

Researchers conducting the study are required to file informed consent before the study begins.

How to fill out informed consent in research?

Informed consent forms typically include detailed information about the study, risks and benefits, participant rights, and contact information for questions. Participants are required to read and sign the form to indicate their consent.

What is the purpose of informed consent in research?

The purpose of informed consent in research is to ensure that participants are aware of the study details, risks involved, and their rights, allowing them to make an informed decision about participating.

What information must be reported on informed consent in research?

Informed consent forms should include study objectives, procedures, risks and benefits, data handling, confidentiality measures, and contact information for queries.

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