Friday, February 17, 2017
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The UL Dietary Supplement Risk Assessment Tool is based on the requirements of the FDA’s 21 CFR Part 111, the Natural Products Association Dietary Supplement Standard and ANSI-NSF 173 Section 8. UL Registrar LLC offers Good Manufacturing Practices audits for Dietary Supplements, Dietary Ingredients, Nutraceuticals, and Natural Products. The tool describes the audit process, audit reporting, the Process Evaluation Assessment of Risk (PEAR) and the risk criteria an audit will be categorized based on the outcome.
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