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Regulations Research

Federal and State Rules,For What You Actually Offer.

Start with your state, then check the federal floor for the services on your menu. Everything here is sourced and dated, and it points to the agency or statute behind it.

Federal summaries current as of October 2026.

01 / By State

Compare Every State

What a clinic has to build depends first on whether your state enforces the corporate practice of medicine. Pick a state to open its guide.

  • Strict CPOM · MSO-PC · 17 states — Physician-owned PC plus an MSO
  • CPOM enforced · 15 states — CPOM enforced, more flexibility
  • Non-CPOM · 18 states — Ownership is freer; a medical director is still required
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Select a state to open its guide. Shading follows each state's corporate practice of medicine classification.

02 / By What You Offer

Browse by Service

Each group starts from the federal rules that apply and links to our guides on how states layer their own requirements on top.

Compounded Drugs and Peptides

FDA compounding rules (section 503A for patient-specific prescriptions, 503B for registered outsourcing facilities) plus state pharmacy law.

Hormones and Controlled Substances

Prescription drug rules, DEA scheduling for controlled substances such as testosterone, and state controlled-substance and telehealth rules.

Aesthetics and Devices

Prescription neuromodulators and fillers, FDA-regulated devices, and state delegation and scope-of-practice rules for who may inject or operate lasers.

IV Therapy and Infusions

Prescription fluids and additives, pharmacy and nursing scope rules, and in some states IV-specific statutes.

Ownership, Structure and Staffing

State corporate practice of medicine doctrine, professional-entity statutes, fee-splitting rules and nurse practitioner and physician assistant scope.

04 / The Federal Floor

What Applies in Every State

Federal rules set the minimum. States can and often do add to them. Summaries are current as of October 2026; the linked sources control if anything has changed.

503A and 503B Compounding

Section 503A covers state-licensed pharmacies compounding for an identified patient under a prescription. Section 503B covers FDA-registered outsourcing facilities, which can compound without patient-specific prescriptions but must meet current good manufacturing practice. Which lane a product comes from decides what a clinic can lawfully stock and administer.

As of October 2026

GLP-1 Compounding

FDA resolved the tirzepatide shortage in December 2024 and the semaglutide shortage in February 2025, and shortage-based compounding discretion has ended. FDA said in February 2026 that it intends to restrict GLP-1 active ingredients in mass-marketed compounded drugs and to act against ads claiming a compounded drug is the same as, or as proven as, the approved one. In April 2026 it proposed excluding semaglutide, tirzepatide and liraglutide from the 503B bulks list. That proposal was not final when we last checked.

As of October 2026

Peptides

Removal of a peptide from FDA's Category 2 list does not make it compoundable. In July 2026 FDA's compounding advisory committee voted to recommend adding BPC-157 and some other peptides to the 503A bulks list. That vote is advisory, FDA staff opposed adding BPC-157, and we found no final FDA action. Products sold as "research use only" are not for human use, whatever the label implies.

As of October 2026

Telemedicine and Controlled Substances

DEA flexibilities that allow prescribing controlled substances, including testosterone, by telemedicine without a prior in-person visit run through December 31, 2026. A permanent special-registration rule has not been finalized as far as we could confirm, so plan for the possibility that in-person requirements return on January 1, 2027.

As of October 2026

Menopausal Hormone Therapy Labeling

FDA announced in November 2025 that it was removing boxed warnings on cardiovascular disease, breast cancer and dementia from menopausal hormone therapy labels, and approved label changes for several products in February 2026. The endometrial cancer warning remains.

As of October 2026

Health Claims and Advertising

The FTC expects health claims to be supported by competent and reliable scientific evidence, and its staff guidance emphasizes randomized controlled human trials for benefit claims. FDA separately treats claims that a product treats a disease as drug claims. Clinics are responsible for their own marketing, including claims made on their behalf.

As of October 2026

Adverse Event Reporting

Serious adverse events involving drugs and devices can be reported to FDA through MedWatch. Clinics should also have an internal process for recording and escalating adverse events to their medical director.

As of October 2026
05 / Official Databases

Check the Source Yourself

Where the rule lives in a database or a registry, go to the agency. These are the ones we use most.

Next Step

Rules Checked. Now Build on Them.

A clinic that fits its state's rules starts with a physician licensed there, a structure that matches the law and protocols for every service. We connect you with all three.

This page is educational and not legal advice. Laws, rules and agency positions change, and a state's rule can differ from the summary here. Confirm with the cited agency or with licensed healthcare counsel in your state before acting. Spot something out of date?Tell us.