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Development of FDA-regulated medical products : a translational approach

Whitmore, Elaine, author.
Milwaukee, Wisconsin : ASQ Quality Press, 2012. 2012

High-confidence medical devices cyber-physical systems for 21st century health care : a research and

Arlington, Va. : U.S. Networking and Information Technology Research and Development Program, National Coordination Office, [2009] 2009

Medical devices and the public's health the FDA 510(k) clearance process at 35 years

Institute of Medicine (U.S.)
Washington, D.C. : National Academies Press, 2011. 2011

Medical devices are current regulations doing enough for patients? : hearing before the Subcommittee

United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health.
Washington : U.S. G.P.O. : For sale by the Supt. of Docs., U.S. G.P.O., 2012. 2012

Medical devices FDA should expand Its consideration of information security for certain types of dev

United States. Government Accountability Office, author, issuing body.
[Washington, D.C.] : United States Government Accountability Office, 2012. 2012

Medical devices FDA should take steps to ensure that high-risk device types are approved through the

United States. Government Accountability Office.
[Washington, D.C.] : U.S. Govt. Accountability Office, [2009] 2009

Assurance of sterility for sensitive combination products and materials : new paradigms to bring inn

London : Academic Press, ©2020. 2020