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Review a completed Form FDA 1572 before it goes to the sponsor
Review an informed consent form against 21 CFR 50.25 and 45 CFR 46.116
Check a protocol against the IRB approval criteria before it is submitted
Draft the follow-up letter after a monitoring visit
Review a prompt before you send it
Review a prompt bound for a reasoning model
Review a tool definition an agent will call
Put the instruction first, and fence the material