Also called recovery validation, it confirms your test method can actually recover the specific organisms in your specific product matrix. USP <64> requires it, and it’s the first thing a regulator asks for when a product is challenged.
Skipping it saves a little upfront, but it can produce low total viable counts even when your product is dosed correctly. The result: a product that can’t be released, and a manufacturing problem that’s expensive to unwind.
Run a suitability study on every new formulation. It’s the cheapest insurance you’ll buy.
We design recovery strategies built around your product, not pulled from a catalogue. If you’re scaling, reformulating, or prepping for an audit, that work pays for itself.
Learn more → https://lnkd.in/gcYm2bxZ
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