Built to USP standards — and happy to prove it.
Quality isn't a badge on a wall. It's the rooms we compound in, the ingredients we accept, the tests we run and the documentation we hand you with every lot.
Verified ingredients
Active ingredients only from FDA-registered suppliers, each lot quarantined and identity-verified on receipt before it is released to compounding.
Non-sterile compounding
Capsules, creams, troches and suspensions prepared in a dedicated, environmentally controlled room with documented cleaning logs.
Sterile compounding
ISO 7 buffer room with ISO 5 primary engineering controls. Routine viable air and surface sampling; staff media-fill and glove-tip tested.
Hazardous drug handling
Negative-pressure containment room with externally vented C-PEC, protecting staff and preventing cross-contamination of other preparations.
Pharmacist sign-off
Nothing ships until a pharmacist reviews the test results, the compounding record and the final label against the original prescription.
Independent laboratories
Potency, sterility and endotoxin testing by FDA-registered, DEA-licensed third-party labs. Certificates of analysis available for every lot.
Facility imagery is illustrative.