GxP 101: Creating a Workable User Requirement Specification (URS) for Your Life Science Facility

GxP 101: Creating a Workable User Requirement Specification (URS) for Your Life Science Facility

New and growing life science facilities need to understand GMP/GDP requirements that are imperative to regulatory compliance and smooth running operations. Walk though setting up an effective URS that will help you identify a Validation Master Plan and DQ/IQ/OQ/PQ needs, using examples of manufacturing and logistics facilities.

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