Manufacturer testing is a starting point, not a standard. Wild Rose independently re-verifies every lot through two Canadian laboratories before a single vial is labelled. Here's exactly how it works.
We begin by obtaining written confirmation of the lot number and production records directly from the manufacturer, along with their third-party testing results. We review every figure they provide - but we don't stop there. Manufacturer testing isn't good enough for us, and it shouldn't be for you.
We send samples from the lot to the University of Alberta, where the material undergoes mass spectrometry to confirm identity and HPLC to measure purity. This verifies that the compound is exactly what it claims to be - and exactly how pure.
From the same lot, we send a separate series of samples to PBR for endotoxin screening. Same lot, two independent labs, two distinct layers of verification.
Once testing is complete, we reprint every label with the correct lot number and match each lot directly to its laboratory results. The number on the vial ties to the testing for that specific lot - nothing generic, nothing recycled.
Every Certificate of Analysis (COA) is published on our website, front and centre - the current lot's results are shown first so they're easy to find. Previous lot results are never deleted; they stay archived in the banner below, so anyone can trace our full testing history. Look up any lot number to pull the complete record for the exact product in your hand - nothing hidden, nothing overwritten.
Each finished label carries a lot number that ties back to its own report record: lot number, product, laboratory result, report date, version, and report file. Enter that number on the lookup page to open the report for the product in your hand.
Open lot lookupThe lookup is powered by the live COA archive rather than hardcoded sample rows, so published reports stay current on every surface.
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