{"id":290,"date":"2021-06-15T11:08:48","date_gmt":"2021-06-15T11:08:48","guid":{"rendered":"https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/?post_type=event&#038;p=290"},"modified":"2021-06-15T11:23:34","modified_gmt":"2021-06-15T11:23:34","slug":"usfda-iacra-webinar-series-on-medical-device-iso-13485-and-mdsap","status":"publish","type":"event","link":"https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/coalition-action\/events\/usfda-iacra-webinar-series-on-medical-device-iso-13485-and-mdsap\/","title":{"rendered":"USFDA &#8211; IACRA Webinar Series on Medical Device: ISO 13485 and MDSAP"},"content":{"rendered":"\n<p>The United States Food and Drug Administration (FDA) with the support of the <a href=\"\/regulatory-convergence\/projects\/standards-alliance\/2-0\/\">Medical Device Regulatory Convergence Project<\/a> co-lead by USAID, ANSI, and AdvaMed through the <a href=\"\/regulatory-convergence\/\">Inter-American Coalition for Regulatory Convergence in the Medical Technology Sector<\/a>, organized a series of webinar sessions on ISO 13485 and Medical Device Single Audit Program (MDSAP) outcomes utilization for regulatory purposes, where ANVISA and ANMAT, besides the USFDA share their experiences.<\/p>\n","protected":false},"featured_media":0,"parent":0,"template":"","event_category":[10],"class_list":["post-290","event","type-event","status-publish","hentry","event_category-public","event_category-10","description-off"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.4 - 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