Wisconsin good-faith exam for med spas

Requirements for the good-faith examination before treatment. Below are the Wisconsin rules that govern it, each linked to its primary source.

Good-faith examination in Wisconsin

Wisconsin imposes an informed consent duty by statute and measures it against a reasonable-physician standard — and its telemedicine rules refuse to lower any of it.

  • Any physician who treats a patient shall inform the patient about the availability of reasonable alternate medical modes of treatment and about the benefits and risks of those treatments. The measure is the reasonable physician standard — disclosure of what a reasonable physician in the same or a similar specialty would know and disclose in the circumstances.

    Wis. Stat. § 448.30 · verified Sep 2, 2026

  • The statute also names what the duty does NOT require, which is where a practice usually over- or under-discloses: detailed technical information a patient would in all probability not understand; risks apparent or already known to the patient; extremely remote possibilities that might falsely or detrimentally alarm them; and information in emergencies where withholding treatment would be more harmful.

    Wis. Stat. § 448.30(2)–(5) · verified Sep 2, 2026

  • A physician-patient relationship MAY be established through telemedicine, but nothing about the channel changes the duty: a physician is held to the same standards of practice and conduct, including patient confidentiality and recordkeeping, whether services are provided in person or by telemedicine — and must be licensed by the Wisconsin board to treat a patient located in this state.

    Wis. Admin. Code Med §§ 24.03, 24.04 and 24.05 · verified Sep 2, 2026

  • The physician also owns the equipment question: a physician providing services by telemedicine is responsible for the quality and safe use of the equipment and technology integral to diagnosis and treatment. Responsibility for the tooling is not delegable to whoever supplied it.

    Wis. Admin. Code Med § 24.06 · verified Sep 2, 2026

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MedSpaRadar is regulatory monitoring and reference: it summarizes public laws, regulations and agency actions and links each to its source. It is not legal, medical, or compliance advice, and using it creates no attorney-client relationship. A summary can lag its source or leave out detail, and monitoring itself can be interrupted — so an absence of alerts means nothing reached you, not that nothing happened. Read the cited source, check its effective date, and confirm any change to your operations or clinical practice with qualified health-law counsel and your medical director.