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Regulatory

Informed consent

The process of explaining a procedure's risks, benefits, and alternatives before agreement.

Informed consent involves discussion of: the procedure, its risks (common and rare), benefits, alternatives, and what happens if no treatment occurs. It must be documented in writing.

What this means for you: review the consent document before signing. Don't sign in haste — bring a translator or advocate if needed.

General information, not medical advice

What a term means for you depends on your own reports. Ask your treating doctor, or send your reports for a free review.

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