This page lists three turns, the messages you send to the AI one after another in the same chat, and then a check of the answer. Keep it open next to your chat. Each turn shows the next thing to paste, with the values you entered already filled in. Nothing is sent from this page, and your conversation stays in the AI tool you are using.
The complete current form, including signature block, interpreter attestation, and any back-page authorizations.
Research consent follows a different regime: key information first, no exculpatory language.
The state, plus which disclosure standard applies if you know it: physician-based or reasonable-patient.
The patient population, target reading level, languages, and who signs when the patient cannot.
Anything risk management, the carrier, an IRB, or a statute requires word for word.
Watch for these throughout
Informed consent standards, and whether a state prescribes form content for particular procedures, vary by state and change. Confirm the governing standard yourself. Treat anything the model says about it as unverified.
The model will supply complication percentages that sound right and are invented. Every number in the final form must come from the clinical team.
Simplifying a risk statement can narrow the disclosure. Read the cut list and the side-by-side log line by line before adopting anything.
Research consent under the Common Rule is a different regime with its own key-information and non-exculpatory requirements. Do not run a research form through a treatment-consent edit.
A translated form must be re-verified after any English change. Rewriting the English silently desynchronizes every translation you have.