October 31 – November 1, 2018Minneapolis Convention CenterMinneapolis, MN


PLM software designed to automate business processes and manage data for FDA regulatory compliance. Integrated modules and a centralized repository facilitate quality control and audit/inspection requirements using built-in forms and reporting functionality including: CAPA, DMR, DHF & DHR reporting, and manage non-conformance tracking in the CMPRO As-Built module.

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