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International Medical Device Regulators Forum (IMDRF) is a global group of medical device regulators working together to regulate medical products in various countries.
Member of the IMDRF include: Therapeutic Goods Administration (Australia), National health Surveillance Agency (Brazil), Health Canada (Canada), China Food and Drug Administration (China), European Commission Directorate-General for Internet, Market, Industry, Entrepreneurship and SMEs (Europe), Pharmaceuticals and Medical Devices Agency (Japan), Ministry of Health, Labour and Welfare (Japan), Russian Ministry of Health (Russia), Health Sciences Authority (Singapore), U.S. Food and Drug Administration (United States).