What must a med spa in New Mexico report to the board?
Facility · part of The Practice Perimeter
this part defines the requirements for affected entities to report to the board: (1) payments relating to malpractice actions or claims arising in New Mexico involving licensees and applicants; (2) professional review actions;
16.10.10 NMAC (Reporting requirements for licensees, applicants and other persons and entities) · verified Sep 4, 2026 · regulatory monitoring, not legal advice
The rest of what New Mexico says on this
Every other rule we have verified under med-spa registration & licensing, each linked to its primary source.
“Aesthetic healthcare facility” means a business or other practice that provides aesthetic healthcare procedures to the general public .
16.12.14.7(A)(3) NMAC (Definitions; eff. 2024-05-21) · verified Sep 4, 2026
Every patient encounter in an aesthetic healthcare facility must generate a healthcare record.
16.12.14.11(A) NMAC (Patient records, confidentiality, and advertising) · verified Sep 4, 2026
⛔ NEW MEXICO PUBLISHES THE COST OF ENTRY AS A FEE RULE, SO THIS IS THE PRICE RATHER THAN AN ESTIMATE. 16.34.14.8 FEES: The board or department, where applicable, may charge the following fees: A. Enterprise or establishment license (original): $200.00 B. Enterprise or establishment license (renewal): $50.00. A School license (original and renewal) is $500.00. Part 14 exists to set fees; the civil penalties in Part 15 are a different instrument and are not what it costs to open.
16.34.14.8 NMAC (⛔ the establishment fee a new studio actually pays) · verified Sep 7, 2026
⛔ NEW MEXICO LETS A PHARMACY COMPOUND A COMMERCIALLY AVAILABLE PRODUCT FOR DISPENSING ONLY ON STATED CONDITIONS, WHICH IS THE COMPOUNDED-SEMAGLUTIDE QUESTION IN ONE PARAGRAPH. Commercially available product may be compounded for dispensing to individual patients provided the following conditions are met: (a) the commercial product is not reasonably available from normal distribution channels in a timely manner to meet patient’s needs; and (b) the prescribing practitioner has requested that the drug be compounded; or (c) if the compounded product is changed to produce for that patient a significant difference, as authorized by the prescriber, between the compounded drug and the comparable commercially available drug product, or if use of the compounded product is in the best interest of the patient; when a compounded product is to be dispensed in place of a commercially available product, the prescriber and patient shall be informed that the product will be compounded.
16.19.30.9(A)(3) NMAC (Compounding of Non-Sterile Pharmaceuticals — commercially available products) · verified Sep 8, 2026
Non-sterile drug products may be compounded in licensed pharmacies as a result of a practitioner’s prescription order based on the practitioner-patient-pharmacist relationship in the course of professional practice. (2) Preparing limited quantities of prescription drug orders in anticipation based upon a history of receiving valid prescriptions issued within an established practitioner-patient-pharmacist relationship in the course of professional practice.
16.19.30.9(A)(1)-(2) NMAC (Compounding of Non-Sterile Pharmaceuticals — general requirements) · verified Sep 8, 2026
How other states answer this
- Alabama
- Alaska
- Arizona
- Arkansas
- Delaware
- Florida
- Georgia
- Hawaii
- Idaho
- Illinois
- Indiana
- Iowa
- Kansas
- Massachusetts
- Michigan
- Minnesota
- Mississippi
- New Jersey
- Ohio
- Pennsylvania
- Texas
- West Virginia
Related New Mexico questions
- Does a med spa have to register or hold a license in New Mexico?
- What does it cost to open a med spa in New Mexico?
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← All New Mexico rules and changes · MedSpaRadar is regulatory monitoring and reference, not legal, medical, or compliance advice. Verify against the linked primary source and consult qualified counsel before acting — rules change and turn on your specific facts. Legislative data via LegiScan (CC BY 4.0).