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Wednesday, May 6, 2015
UL_GMPRiskAssessment_2.23.17, 2 MB
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DownloadThe UL Pharmaceutical Drug Audit Tool is based on the requirements of FDA’s 21 CFR Parts 210⁄211. UL GMP Reports and accredited certificates are accepted by multiple brands.
Provides a brief overview of UL's Services across Industries and Markets.
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