Mastering Design Control with Medical Device PLM

Tuesday, January 11, 2022 at 11:00 ET

Join Thomas Skogen from Minerva as we explore design controls for medical devices; an often time consuming and frustrating process that may delay time to market and gaining regulatory approval. See how Design History Files DHF and Device Master Records (DMR) may be successfully managed within a PLM construct. See how templates are used to manage deliverables required for final DHF and DMR creation. Finally, automatic creation of DHFs and DMRs for submittal to governing entities.

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