Integrated safety and risk assessment for medical devices and combination products / by Gad, Shayne C., 1948-, SpringerLink (Online service)

Subjects: “…Medical instruments and apparatus Safety measures.…”
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Statistical methods and analyses for medical devices / by Pardo, Scott, SpringerLink (Online service)

Subjects: “…Medical instruments and apparatus Statistical methods.…”
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Modifications to devices subject to premarket approval (PMA) the PMA supplement decision-making process. by Center for Devices and Radiological Health (U.S.), Center for Biologics Evaluation and Research (U.S.)

Subjects: “…Medical instruments and apparatus Testing.…”
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H.R. 1346, the Medical Device Safety Act of 2009 hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Eleventh C... by United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health

Subjects: “…Products liability Medical instruments and apparatus United States.…”
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Better health care with quality medical devices FDA on the cutting edge of device technology. by United States. Food and Drug Administration. Office of Public Affairs

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FDA medical device approval is there a better way? : hearing before the Subcommittee on Health Care, District of Columbia, Census, and the National Archives of the Committee on Ove... by United States. Congress. House. Committee on Oversight and Government Reform. Subcommittee on Health Care, District of Columbia, Census, and the National Archives

Subjects: “…Medical instruments and apparatus United States Testing.…”
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Quick tips, when getting medical tests by United States. Agency for Healthcare Research and Quality

Subjects: “…Medical instruments and apparatus Testing.…”
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Medical device software verification, validation and compliance by Vogel, David A., ProQuest Ebook Subscriptions, ProQuest (Firm)

Subjects: “…Medical instruments and apparatus Testing.…”
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Inspection of medical devices : for regulatory purposes / by SpringerLink (Online service)

Subjects: “…Medical instruments and apparatus Testing.…”
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Mejor cuidado de la salud con dispositivos médicos de calidad FDA a la cabeza en tecnología de dispositivos médicos. by United States. Food and Drug Administration. Office of Public Affairs

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FDA medical device reviews, evaluation is needed to assure requests for additional information follow a least burdensome approach : report to congressional requesters. by United States. Government Accountability Office

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Assay migration studies for in vitro diagnostic devices by Center for Devices and Radiological Health (U.S.). Office of In Vitro Diagnostic Device Evaluation and Safety, Center for Biologics Evaluation and Research (U.S.)

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Annual report by Center for Devices and Radiological Health (U.S.). Office of Device Evaluation

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In vitro diagnostic (IVD) device studies, frequently asked questions by Center for Devices and Radiological Health (U.S.), Center for Biologics Evaluation and Research (U.S.)

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Food and Drug Administration FDA faces challenges meeting its growing medical product responsibilities and should develop complete estimates of its resource needs : report to congr... by United States. Government Accountability Office

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In vitro diagnostic (IVD) device studies, frequently asked questions by Center for Devices and Radiological Health (U.S.), Center for Biologics Evaluation and Research (U.S.)

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FDA user fees : advancing public health : hearing of the Committee on Health, Education, Labor, and Pensions, United States Senate, One Hundred Twelfth Congress, first session ...... by United States. Congress. Senate. Committee on Health, Education, Labor, and Pensions

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21st century cures : modernizing clinical trials : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Thirteen... by United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health

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Performance report to Congress for the Medical Device User Fee and Modernization Act of 2002 by United States. Food and Drug Administration

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FY ... MDUFMA financial report required by the Medical Device User Fee and Modernization Act of 2002 by United States. Food and Drug Administration

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