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If my company makes different grades (food, cosmetic, drug) of the same ingredient, how will this affect the audit process?

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If my company makes different grades (food, cosmetic, drug) of the same ingredient, how will this affect the audit process?

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The USP Verification Programs cover a broad range of ingredients used in human health care such as drug substances, dietary ingredients used in dietary supplements, and excipients. These Programs differ from each other in respect to the Good Manufacturing Process (GMP).

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