Compliance documents you buy once
No subscription. Pick your state, buy the document, keep it. Each pack is assembled from the same source-linked record that powers the rest of the site — every entry dated and linked to the statute, rule, or federal notice it came from.
What else buys you an answer to this question? An association membership is the usual route: AmSpa Basic is $395/year and AmSpa Plus is $845/year, each including a state legal summary alongside events, webinars and member rates (their published rates, Aug 2026). These packs are one document, bought once, with every entry dated and linked to the statute it came from. The full side-by-side, including when a membership is the better buy →
The Snapshot is credited toward a subscription. Buy it, and if you subscribe within 30 days the $49 comes off. All-Access members already have every pack for their states — there is nothing extra to buy.
One-time packs
The document on file
Source-linked, dated compliance documents for your state — buy once, yours to keep. Included free with All-Access.
Packs always include the federal record; the count is state-specific changes on record.
State Compliance Snapshot
Every published med-spa & injectable change for your state — federal + national too — with the what-to-do, source-linked.
Someone who needs the current record for one state, on paper, today.
- Every published med-spa and injectable change on record for your state, dated
- The federal FDA and Federal Register record that applies in every state
- The "what to do" line for each item, not just what changed
- A direct link to the primary source for every entry, so it can be verified
- Printable — built to hand to a medical director or attorney
$49 one-time
Get Snapshot — $49Peptide & GLP-1 Status Pack
What your state’s law says about a compounded GLP-1 or peptide program, each answer quoted from its statute. Confirmed in 10 states so far — pick your state above to check.
A practice running — or about to run — a compounded GLP-1 or peptide program, that needs its own state’s answer before it orders.
- May a pharmacy supply compounded drugs for office use, or only against a patient-specific prescription — quoted from your state’s own statute or rule
- Whether the pharmacy compounding a sterile injectable needs a separate license or permit
- Whether an out-of-state pharmacy or 503B outsourcing facility must be licensed in your state to supply you
- What changes when the practice dispenses drugs itself rather than administering them
- The federal standings alongside each answer — the same record /tracker publishes free, included so the document stands alone
- Kept current through the February 2027 PCAC review
$99 one-time
Get the Pack — $99Medical Director Pack
Delegation, supervision, good-faith exam, ownership and the disciplinary landscape for your state — statute-cited, plus who on your staff may perform which procedure and up to what limit.
The physician whose name is on a practice they do not run day to day — and the operator preparing for that conversation.
- Physician supervision and delegation, quoted from your state’s own statute or rule
- The good-faith-examination requirement, and who may perform it
- Ownership and corporate-practice-of-medicine limits on how the entity may be structured
- RN and NP scope for injectables, with the supervision each one turns on
- The disciplinary landscape — what the board has actually acted on
- Who on your staff may perform which procedure, and up to what limit, from the scope corpus
- Every limit printed beside the citation it came from, with the exception conditions in full
$197 one-time
Get the Pack — $197MedSpaRadar 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).
Get regulatory changes as they publish
We scan all 50 state legislatures daily, plus the FDA and the Federal Register. Free weekly Brief — what changed, in plain language, with the source.
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