Showing 1 - 20 results of 238 for search '"Medical instruments and apparatus"', query time: 5.07s Refine Results
  1. 1
    Medical devices and equipment competitive conditions affecting U.S. trade in Japan and other principal foreign markets.

    Medical devices and equipment competitive conditions affecting U.S. trade in Japan and other principal foreign markets. by United States International Trade Commission

    Subjects: “…Medical instruments and apparatus industry United States.…”
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  2. 2
    Medical device design and regulation /

    Medical device design and regulation / by DeMarco, Carl T., ProQuest Ebook Subscriptions

    Published: ASQ Quality Press, 2011
    Subjects: “…Medical instruments and apparatus United States.…”
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  3. 3
    FDA regulation of medical devices /

    FDA regulation of medical devices / by Thompson, Bradley Merrill

    Published: Interpharm Press, 1995
    Subjects: “…Medical instruments and apparatus Safety regulations United States.…”
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  4. 4
    FDA's clearance of medical devices through the 510(k) process.

    FDA's clearance of medical devices through the 510(k) process. by United States. Department of Health and Human Services. Office of Inspector General

    Subjects: “…Medical instruments and apparatus Government policy United States.…”
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  5. 5
    Medical devices are current regulations doing enough for patients? : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Eleventh Congress, first session, June 18, 2009.

    Medical devices are current regulations doing enough for patients? : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, On... by United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health

    Published: U.S. G.P.O., 2012
    Subjects: “…Medical instruments and apparatus Safety regulations United States.…”
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  6. 6
    Medicare lack of price transparency may hamper hospitals' ability to be prudent purchasers of implantable medical devices : report to the Chairman, Committee on Finance, U.S. Senate.

    Medicare lack of price transparency may hamper hospitals' ability to be prudent purchasers of implantable medical devices : report to the Chairman, Committee on Finance, U.S. Senat... by United States. Government Accountability Office, United States. Congress. Senate. Committee on Finance

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  7. 7
    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 Congress, first session, May 12, 2009.

    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

    Published: U.S. G.P.O., 2011
    Subjects: “…Products liability Medical instruments and apparatus United States.…”
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  8. 8
    The FDA and worldwide quality system requirements guidebook for medical devices /

    The FDA and worldwide quality system requirements guidebook for medical devices / by Daniel, Amiram, Kimmelman, Ed, ProQuest Ebook Subscriptions

    Published: ASQ Quality Press, 2008
    Subjects: “…Medical instruments and apparatus industry Law and legislation United States.…”
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  9. 9
    Protecting patients from defective medical devices hearing of the Committee on Health Education, Labor, and Pensions, United States Senate, One Hundred Eleventh Congress, first session, on examining S. 540, to amend the Federal Food, Drug, and Cosmetic Act with respect to liability under state and local requirements respecting devices, August 4, 2009.

    Protecting patients from defective medical devices hearing of the Committee on Health Education, Labor, and Pensions, United States Senate, One Hundred Eleventh Congress, first ses... by United States. Congress. Senate. Committee on Health, Education, Labor, and Pensions

    Published: U.S. G.P.O., 2011
    Subjects: “…Products liability Medical instruments and apparatus United States.…”
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  10. 10
    Protect Medical Innovation Act of 2012 report together with dissenting views (to accompany H.R. 436) (including cost estimate of the Congressional Budget Office).

    Protect Medical Innovation Act of 2012 report together with dissenting views (to accompany H.R. 436) (including cost estimate of the Congressional Budget Office). by United States. Congress. House. Committee on Ways and Means

    Published: U.S. G.P.O., 2012
    Subjects: “…Medical instruments and apparatus Taxation Law and legislation United States.…”
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  11. 11
    Medical devices FDA faces challenges in conducting inspections of foreign manufacturing establishments : testimony before the Subcommittee on Health, Committee on Energy and Commerce, House of Representatives /

    Medical devices FDA faces challenges in conducting inspections of foreign manufacturing establishments : testimony before the Subcommittee on Health, Committee on Energy and Commer... by Crosse, Marcia, United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health, United States. Government Accountability Office

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  12. 12
    Protect Medical Innovation Act of 2015 : report together with minority views (to accompany H.R. 160) (including cost estimate of the Congressional Budget Office).

    Protect Medical Innovation Act of 2015 : report together with minority views (to accompany H.R. 160) (including cost estimate of the Congressional Budget Office). by United States. Congress. House. Committee on Ways and Means

    Subjects: “…Medical instruments and apparatus Taxation Law and legislation United States.…”
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  13. 13
    Better health care with quality medical devices FDA on the cutting edge of device technology.

    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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  14. 14
    Medical devices and the public's health the FDA 510(k) clearance process at 35 years /

    Medical devices and the public's health the FDA 510(k) clearance process at 35 years / by Institute of Medicine (U.S.), ProQuest Ebook Subscriptions, National Research Council (U.S.). Committee on the Public Health Effectiveness of the FDA 501(k) Clearance Process, Institute of Medicine (U.S.). Board on Population Health and Public Health Practice, ProQuest (Firm)

    Published: National Academies Press, 2011
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  15. 15
    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 Oversight and Government Reform, House of Representatives, One Hundred Twelfth Congress, first session, June 2, 2011.

    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

    Published: U.S. G.P.O., 2011
    Subjects: “…Medical instruments and apparatus United States Testing.…”
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  16. 16
    Guidance for industry and FDA staff expedited review of premarket submissions for devices.

    Guidance for industry and FDA staff expedited review of premarket submissions for devices. by Center for Devices and Radiological Health (U.S.), Center for Biologics Evaluation and Research (U.S.)

    Subjects: “…Medical instruments and apparatus United States Evaluation.…”
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  17. 17
    Annual reports for approved premarket approval applications (PMA)

    Annual reports for approved premarket approval applications (PMA) by Center for Devices and Radiological Health (U.S.), Center for Biologics Evaluation and Research (U.S.)

    Subjects: “…Medical instruments and apparatus Evaluation United States.…”
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  18. 18
    Requests for inspection by an accredited person under the Inspection by Accredited Persons Program authorized by Section 201 of the Medical Device User Fee and Modernization Act of 2002

    Requests for inspection by an accredited person under the Inspection by Accredited Persons Program authorized by Section 201 of the Medical Device User Fee and Modernization Act of... by Center for Devices and Radiological Health (U.S.), Center for Biologics Evaluation and Research (U.S.)

    Subjects: “…Medical instruments and apparatus Inspection United States.…”
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  19. 19
    Letters and certificates recommending the patent portable warm and hot bath to which are added explanations of the nature of the remedy and instructions for its application, designating some of the cases in which it will be particularly beneficial ... /

    Letters and certificates recommending the patent portable warm and hot bath to which are added explanations of the nature of the remedy and instructions for its application, design... by Jennings, Samuel K. (Samuel Kennedy), 1771-1854

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  20. 20
    The impact of medical device and drug regulation on innovation, jobs, and patients a local perspective : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Twelfth Congress, first session, September 26, 2011.

    The impact of medical device and drug regulation on innovation, jobs, and patients a local perspective : hearing before the Subcommittee on Health of the Committee on Energy and Co... by United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health

    Published: U.S. G.P.O., 2012
    Subjects: “…Medical instruments and apparatus Safety regulations United States.…”
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