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Wednesday, May 6, 2015

UL_GMPRiskAssessment_2.23.17, 2 MB

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UL Registrar LLC’s Pharmaceutical Risk Assessment Tool is based strictly on the requirements of FDA’s 21 CFR Parts 210–211. The audit tool describes the audit process, the Process Evaluation Assessment of Risk (PEAR) and the risk scoring criteria.

Provides a brief overview of UL's Services across Industries and Markets.

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