Medical Device Complaints & CAPA
March 9, 2021 - CA USPanelcompliance
panelcompliance@gmail.com
Phone:8004479407
Overview: This webinar will explain the CAPA process from information gathering through MDR and Recall decision making to final CAPA closing. Post closing effectiveness evaluation is required and will be explained. Preventative Action is often neglected and will be discussed. Post distribution product monitoring including customer surveys will be explained. Integration of manufacturing non conformaties with the CAPA program will be discussed.
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