Seven steps. No improvisation.

A medical questionnaire covering history, goals, current medications, and contraindications — reviewed in full before anything else happens.

The intake screens for the conditions that make each peptide class unsafe — malignancy history, pregnancy, cardiovascular disease, drug interactions — and puts every answer in front of the physician who decides.

“Is this just a form that rubber-stamps a sale?” No. It exists to disqualify people for whom a protocol is wrong, before a physician ever spends time on the file.

A single draw at a partner laboratory near you. A comprehensive panel across the systems a protocol can touch — cardiac, hormonal, metabolic, hepatic, renal — establishing your baseline.

Three panel tiers — Basic, Full, and Elite — matched to what a protocol actually requires. A GH-axis peptide mandates IGF-1; a metabolic protocol pulls insulin, HOMA-IR, and ApoB. You are billed for the markers your protocol reads.

“Why can’t I skip the labs?” Because without a baseline there is nothing to compare the retest against — and the retest is the entire point.

A licensed U.S. physician reads your intake against your markers. If a protocol is appropriate, it is prescribed. If it is not, you are told so plainly.

A physician is the only party who can authorize a prescription here, and that authority sits with them alone. Some intakes end at this step with “not a candidate,” and that outcome carries no charge.

“Is there really a doctor, or a checkbox?” A named, state-licensed physician owns the decision and the liability for it.

Prescriptions are compounded for you in a state-licensed 503A pharmacy — batch-documented and prescription-only.

503A pharmacies compound to an individual prescription under state board oversight. Every batch is documented. This is the same regulatory class that prepares countless everyday prescriptions.

“Where does the actual medication come from?” A licensed U.S. compounding pharmacy, preparing your vial against your specific prescription, batch by documented batch.

Temperature-controlled from pharmacy to your door, in discreet, unbranded packaging.

Peptides are temperature-sensitive; a broken cold chain is a dead protocol. Shipments are packed to hold temperature in transit and arrive without anything on the box that announces what’s inside.

“Will it be obvious what this is?” No. The packaging is deliberately anonymous.

Markers, reference ranges, trends, your active protocol, and physician messaging — in one place.

Every number sits next to its range and its trend line, so you read direction, not just a snapshot. Questions to your physician run through the same portal — no phone tag.

“Do I just get a vial and silence?” No — you get the data, the trend, and a line to the physician who owns it.

Your panel is drawn again. The trend is placed next to the protocol, and a physician decides what changes.

This is the step the rest of the market skips. The same markers are re-drawn, the movement is read against your protocol, and the physician holds, adjusts, or tapers accordingly. The loop is the product — not the vial.

“What am I actually paying for?” Ongoing physician oversight, anchored to your own labs and re-read every 90 days.