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About MDIC: The Medical Device Information Center (MDIC) is a leader in medical device communications, with robust, first-class standards, safety rulemaking, and regulation services. While at times a partner to industry, MDIC is a key resource for all stakeholders, including the FDA, to advance health IT through regulatory and policy-related initiatives.
About MITRE: Commercial sector software development is complex and error-prone, leading to costly maintenance and support problems. Mitre plays a role in the public and private sectors by serving as a trusted advisor to government, industry, and other organizations by delivering hours of free sector-specific training to educate and equip them with the critical expertise needed to build better, safer products in a market-like, secure, and disciplined environment.
About MDIC Origin: In the 1970’s, the United States Department of Health, Education and Welfare (HEW) was working to harmonize U.S. licensing requirements for medical devices. In response, the Center of Devices and Radiological Health (CDRH) was founded in 1977 to serve as an interagency single source for medical device regulations, standards, and information. In 1998, CDRH became the Center for Devices and Radiological Health (CDRH) at the U.S. Food and Drug Administration (FDA), where it continues to fulfill the role of its previous creation. d2c66b5586