— Practitioner Program · Verified-account access
Pharmacy-grade compounds.
Built for your practice.
A verified-account program for licensed practitioners. Practices save an average ~30% on compound cost versus their previous supplier — margin added straight back into the practice. Pharmacy-grade. HPLC ≥99% per lot. COA with every shipment. Shipped from Dallas in 48 hours.
Texas practices sourcing through Merit
certified · sterile-filled facility
HPLC purity, released per lot
shipped from Dallas · no MOQ
— 01 · The economics
Keep your pricing.
Change your margin.
Practices that move their sourcing to Merit cut their average compound cost by roughly 30% versus their previous supplier — without changing a single patient price. That spread stops going to a middleman. It goes back into your practice.
- Don't change your protocols. Same compounds, same doses, same patient programs. Only the invoice changes.
- Don't change your patient pricing. The ~30% isn’t a discount you pass on — it’s margin you’re currently handing your supplier.
- Don't change your workflow. Order office stock, reorder from history, COA on every shipment. Switching is a sourcing decision, not an operational one.
— What 30% looks like
Illustrative example. Actual savings depend on your volume and current supplier. Account pricing is set in your portal at approval — standard or custom to your practice.
Keep the 30%.
License + NPI verified within one business day. No commitments, no activation fees.
— 02 · How we’re different
Sourcing that holds up
to whoever asks.
Overseas synthesis. TFA counterions. No release testing. We don’t. The compound you order is characterized and released to the same standards used by hospital pharmacies — from a US-licensed pharmacy team you can name.
— Sourcing
USP <797> + ISO certified
Active ingredients sourced from a US facility with USP <797> sterile processing and ISO certifications — pharmacist-released, lot-documented, and fully traceable.
— Characterization
HPLC ≥99% per lot
Every batch released only after HPLC purity, sterility (USP <71>), endotoxin (USP <85>), and particulate (USP <788>) testing. COA accompanies every shipment — lot # on every label.
— Counterion
Acetate, not TFA
We exchange to acetate — the salt form used in characterized pharmaceutical references. Most discount sources ship as the trifluoroacetate (TFA) salt because the acetate exchange step is expensive. We do it anyway.
— Not ready to apply yet?
Get The Practice Owner’s Guide to Adding Compounds — the margin math, the compliance basics, and the protocols practices start with. A short email series. Unsubscribe anytime.
— 03 · Apply
Apply for portal access.
License + NPI verification within 1 business day. Approved practitioners get portal access with their account-tier pricing already applied. No commitments, no activation fees.