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Subjects (1-7 of 7)
Medical Instruments And Apparatus Standards United States
1
Development of FDA-regulated medical products : a translational approach
Whitmore, Elaine, author.
Milwaukee, Wisconsin : ASQ Quality Press, 2012. 2012
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OPAC Message
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Axe EBSCO Medical Collection E-Book
Electronic Book
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2
ElectronicResource GovDoc
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
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Axe Federal Documents Online
PREX 23.2:M 46
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3
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
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Axe ProQuest E-Book
Electronic Book
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4
ElectronicResource GovDoc
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
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Axe Federal Documents Online
Y 4.C 73/8:111-52
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5
ElectronicResource GovDoc
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
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Axe Federal Documents Online
GA 1.13:GAO-12-816
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Available
6
ElectronicResource GovDoc
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
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Axe Federal Documents Online
GA 1.13:GAO-09-190
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Medical Instruments And Apparatus Sterilization
7
Assurance of sterility for sensitive combination products and materials : new paradigms to bring inn
London : Academic Press, ©2020. 2020
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Axe Elsevier ScienceDirect Ebook
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