USFDA – IACRA Webinar Series on Medical Device: ISO 13485 and MDSAP

The United States Food and Drug Administration (FDA) with the support of the Medical Device Regulatory Convergence Project co-lead by USAID, ANSI, and AdvaMed through the Inter-American Coalition for Regulatory Convergence in the Medical Technology Sector, 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.