What is a Certificate of Analysis.
A Certificate of Analysis (COA) is a document issued by an independent testing laboratory confirming that a specific lot of compounded medication meets required standards for identity, purity, sterility, and potency. It is the same documentation required of every FDA-registered compounding pharmacy.
Your batch number is printed on the vial label shipped with your protocol. Enter it above to view the third-party test results for the exact batch used in your medication.
What we test for.
IDENTITY AND PURITY
Confirms the compound is what it claims to be and contains no undeclared substances. Tested via HPLC or mass spectrometry. Target: >99% purity.
STERILITY
Confirms the absence of microbial contamination in injectable preparations. Tested per USP <71>. Required for every injectable lot.
POTENCY
Confirms the compound concentration matches the labeled dose within pharmacopeial limits. You receive what the label says.
ENDOTOXIN
Bacterial endotoxin testing per USP <85> for injectable compounds. Below threshold means the preparation is safe for injection.