Explore all of ul.com

Wednesday, May 6, 2015

Thumbnail cover - UL Registrar Pharmaceutical Drug Audit Tool

UL_GMPRiskAssessment_2.23.17, 2 MB

To view this content, please provide your contact information.

Thank you! Here's your document.


The UL Pharmaceutical Drug Audit Tool is based on the requirements of FDA’s 21 CFR Parts 210211. UL GMP Reports and accredited certificates are accepted by multiple brands. 

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