Everyone who sells or makes a supplement or food, or an ingredient, is subject to FDA requirements.
By now, most folks in the FDA-regulated world know the minimum level of cGMPs (current Good Manufacturing Practices). It includes things like raw material testing, specifications, batch records and finished product testing.
But how do you know when your manufacturer has gone from meeting the minimum basic GMPs to the next level—what we can call Excellent Manufacturing Practices, or EMPs?
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