What must a med spa in Indiana report to the board?

Facility · part of The Practice Perimeter

Short answer
Serious adverse events — a patient death, a life-threatening event, or a hospitalization or its prolongation — must be reported to the board within 15 days.

A medical spa must notify the board within 15 days of a patient’s serious adverse event (a death, a life-threatening event, or a hospitalization or its prolongation).

Ind. Code §25-22.5-12.5-6 (SEA 282, 2026) · verified Jul 26, 2026 · regulatory monitoring, not legal advice

Related Indiana rules

  • In Indiana, compounding is pharmacy practice by definition. The practice of pharmacy is performed by a pharmacist — or by a pharmacist intern or an unlicensed person the pharmacist SUPERVISES under section 18.5 — and it includes “the compounding, labeling, administering, dispensing, or selling of drugs and devices … whether dispensed under a practitioner’s prescription or drug order or sold or given directly to the ultimate consumer”, together with their proper and safe storage and distribution and the maintenance of records of receipt, storage, sale and dispensing.

    Ind. Code § 25-26-13-11 · verified Sep 2, 2026

  • ⚠️ and the statute itself sets no compounding standard — it delegates one. In full: “THE BOARD MAY ADOPT A RULE UNDER IC 4-22-2 concerning pharmacies that perform compounding.” Chapter 25-26-13 was read in full for this entry and contains no quantity limit, no office-use permission and no sterile-compounding standard. Whatever governs those in Indiana is in the Board of Pharmacy’s rules, which are published on a page that serves no readable text to us — so nothing is claimed about them here.

    Ind. Code § 25-26-13-4.4 · verified Sep 2, 2026

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← All Indiana rules and changes · 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. Legislative data via LegiScan (CC BY 4.0).