Medical instruments and apparatus -- Safety regulations -- United States

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The concept Medical instruments and apparatus -- Safety regulations -- United States represents the subject, aboutness, idea or notion of resources found in Indiana State Library.

The Resource Medical instruments and apparatus -- Safety regulations -- United States

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Medical instruments and apparatus

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47 Items that share the Concept Medical instruments and apparatus -- Safety regulations -- United States

Safe Medical Devices Act of 1990 : conference report (to accompany H.R. 3095)

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Safe Medical Devices Act of 1990 : report (to accompany H.R. 3095) (including cost estimate of the Congressional Budget Office)

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A delicate balance : FDA and the reform of the medical device approval process : hearing before the Special Committee on Aging, United States Senate, One Hundred Twelfth Congress, first session, Washington, DC, April 13, 2011

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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

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Tools for compliance for the medical device and in vitrol diagnostic product industries

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An overview of the medical device reporting regulation : final rule, effective December 13, 1984, 21 CFR part 803

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Discussion draft of the Food and Drug Administration Globalization Act legislation : device and cosmetic safety provisions : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, second session, May 14, 2008

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Ensuring safe medicines and medical devices for children : hearing of the Committee on Health, Education, Labor, and Pensions, United States Senate, One Hundred Tenth Congress, first session, on examining ensuring safe medicines and medical devices for children, March 27, 2007

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Everything you always wanted to know about the medical device amendments : and weren't afraid to ask

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FDA and the medical device industry : hearings before the Subcommittee on Oversight and Investigations of the Committee on Energy and Commerce, House of Representatives, One Hundred Second Congress, second session, March 25 and June 3, 1992

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FDA's drug and device review process : hearing before the Subcommittee on Oversight and Investigations of the Committee on Energy and Commerce, House of Representatives, One Hundred Second Congress, second session, February 6, 1992

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Federal Food, Drug, and Cosmetic Act : report (to accompany S. 3006)

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Federal policies and the medical devices industry

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Filthy food, dubious drugs, and defective devices : the legacy of FDA's antiquated statute : a staff report, prepared for the use of the Subcommittee on Oversight and Investigations of the Committee on Energy and Commerce, U.S. House of Representatives

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Food and Drug enforcement standards for medical devices : joint hearing before the Subcommittee on Human Resources and Intergovernmental Relations and the Subcommittee on National Economic Growth, Natural Resources, and Regulatory Affairs of the Committee on Government Reform and Oversight, House of Representatives, One Hundred Fourth Congress, first session, September 14, 1995

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Food, Drug, Cosmetic, and Device Enforcement Authorities Act : hearing of the Committee on Labor and Human Resources, United States Senate, One Hundred Second Congress, second session, on S. 2135 ... May 19, 1992

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Food, Drug, Cosmetic, and Device Safety Amendments of 1992 : report together with dissenting views (to acompany H.R. 3642) (including cost estimate of the Congressional Budget Office)

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Import and export regulatory requirements for medical devices, Division of Small Manufacturers Assistance, Office of Training and Assistance

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Import/Export regulatory requirements for medical devices, prepared by Division of Small Manufacturers Assistance, Office of Training and Assistance

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Investigational device exemptions : regulatory requirements for medical devices, prepared by the Division of Small Manufacturers Assistance, Office of Training and Assistance

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Labeling : regulatory requirements for medical devices, prepared by the Division of Small Manufacturers Assistance, Office of Training and Assistance

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Medical Device User Fee Act of 1994 : report together with dissenting and additional views (to accompany H.R. 4864) (including cost estimate of the Congressional Budget Office)

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Medical Device User Fee and Modernization Act of 2002 : report (to accompany H.R. 3580)

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Medical device GMP guidance for FDA investigators, prepared by Division of Small Manufacturers Assistance, Division of Compliance Programs

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Medical device amendments of 1976 : conference report to accompany S. 510

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Medical device amendments of 1976 : report, by the Committee on Interstate and Foreign Commerce to accompany H.R. 11124 together with minority views, February 29, 1976

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Medical device legislation introduced in 93d Congress, prepared by staff for use of Committee on Interstate and Foreign Commerce and its Subcommittee on Public Health and Environment; Aug. 1973

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Medical device legislation pending before Interstate Commerce Commission as of Dec. 15, 1971, together with transmittal letter and summary of administration bill H.R. 12316, prepared by the staff for Subcommittee on Public Health and Environment; Dec. 15, 1971

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Medical device legislation, 1975 : prepared for use of Subcommittee on Health and Environment; July 1975

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Medical device listing information and instructions, prepared by Office of Compliance

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Medical device recalls : an overview and analysis 1983-88 : briefing report to the chairman, Subcommittee on Health and the Environment, Committee on Energy and Commerce, House of Representatives, United States General Accounting Office

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Medical device regulation : too early to assess European system's value as model for FDA : report to the Chairman, Committee on Labor and Human Resources, U.S. Senate, United States General Accounting Office

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Medical device reporting : improvements needed in FDA's system for monitoring problems with approved devices : report to congressional committees, United States General Accounting Office

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Medical device safety : hearings before the Subcommittee on Health and the Environment of the Committee on Energy and Commerce, House of Representatives, One Hundred First Congress, on H.R. 3095 ... November 6, 1989 and July 17, 1990

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Medical devices : FDA can improve oversight of tracking and recall systems : report to the Subcommittee on Oversight and Investigations, Committee on Commerce, House of Representatives, United States General Accounting Office

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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, statement of Marcia Crosse

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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

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Medical devices : hearing before the Committee on Labor and Human Resources, United States Senate, One Hundred First Congress, second session, on examining proposed legislation to revise and strengthen the Food and Drug Administration's regulation of medical devices, July 25, 1990

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Medical devices : protecting patients and promoting innovation : hearing of the Committee on Health, Education, Labor, and Pensions, United States Senate, One Hundred Twelfth Congress, first session ... November 15, 2011

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Preamble compilation : Medical devices, March 1936-March 1978

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Premarket notification, 510(k) : regulatory requirements for medical devices, prepared by Division of Small Manufacturers Assistance, Office of Training and Assistance

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Premarket notification--510(k) : regulatory requirements for medical devices, prepared by Division of Small Manufacturers Assistance, Office of Training and Assistance

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Programs affecting safety and innovation in pediatric therapies : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, first session, May 22, 2007

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Public Law 94-295 : 94th Congress, S. 510, May 28, 1976 : an act to amend the Federal food, drug, and cosmetic act to provide for the safety and effectiveness of medical devices intended for human use, and for other purposes

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Reprocessing of single-use medical devices : hearing of the Committee on Health, Education, Labor, and Pensions, United States Senate, One Hundred Sixth Congress, second session ... June 27, 2000

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A delicate balance : FDA and the reform of the medical device approval process : hearing before the Special Committee on Aging, United States Senate, One Hundred Twelfth Congress, first session, Washington, DC, April 13, 2011
An overview of the medical device reporting regulation : final rule, effective December 13, 1984, 21 CFR part 803
Discussion draft of the Food and Drug Administration Globalization Act legislation : device and cosmetic safety provisions : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, second session, May 14, 2008
Discussion draft of the Food and Drug Administration Globalization Act legislation : device and cosmetic safety provisions : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, second session, May 14, 2008
Ensuring safe medicines and medical devices for children : hearing of the Committee on Health, Education, Labor, and Pensions, United States Senate, One Hundred Tenth Congress, first session, on examining ensuring safe medicines and medical devices for children, March 27, 2007
Everything you always wanted to know about the medical device amendments : and weren't afraid to ask
FDA and the medical device industry : hearings before the Subcommittee on Oversight and Investigations of the Committee on Energy and Commerce, House of Representatives, One Hundred Second Congress, second session, March 25 and June 3, 1992
FDA's drug and device review process : hearing before the Subcommittee on Oversight and Investigations of the Committee on Energy and Commerce, House of Representatives, One Hundred Second Congress, second session, February 6, 1992
Federal Food, Drug, and Cosmetic Act : report (to accompany S. 3006)
Federal policies and the medical devices industry
Filthy food, dubious drugs, and defective devices : the legacy of FDA's antiquated statute : a staff report
Food and Drug enforcement standards for medical devices : joint hearing before the Subcommittee on Human Resources and Intergovernmental Relations and the Subcommittee on National Economic Growth, Natural Resources, and Regulatory Affairs of the Committee on Government Reform and Oversight, House of Representatives, One Hundred Fourth Congress, first session, September 14, 1995
Food, Drug, Cosmetic, and Device Enforcement Authorities Act : hearing of the Committee on Labor and Human Resources, United States Senate, One Hundred Second Congress, second session, on S. 2135 ... May 19, 1992
Food, Drug, Cosmetic, and Device Safety Amendments of 1992 : report together with dissenting views (to acompany H.R. 3642) (including cost estimate of the Congressional Budget Office)
Import and export regulatory requirements for medical devices
Import/Export regulatory requirements for medical devices
Investigational device exemptions : regulatory requirements for medical devices
Labeling : regulatory requirements for medical devices
Medical Device User Fee Act of 1994 : report together with dissenting and additional views (to accompany H.R. 4864) (including cost estimate of the Congressional Budget Office)
Medical Device User Fee and Modernization Act of 2002 : report (to accompany H.R. 3580)
Medical device GMP guidance for FDA investigators
Medical device amendments of 1976 : conference report to accompany S. 510
Medical device amendments of 1976 : report
Medical device legislation introduced in 93d Congress
Medical device legislation pending before Interstate Commerce Commission as of Dec. 15, 1971, together with transmittal letter and summary of administration bill H.R. 12316
Medical device legislation, 1975 : prepared for use of Subcommittee on Health and Environment; July 1975
Medical device listing information and instructions
Medical device recalls : an overview and analysis 1983-88 : briefing report to the chairman, Subcommittee on Health and the Environment, Committee on Energy and Commerce, House of Representatives
Medical device regulation : too early to assess European system's value as model for FDA : report to the Chairman, Committee on Labor and Human Resources, U.S. Senate
Medical device reporting : improvements needed in FDA's system for monitoring problems with approved devices : report to congressional committees
Medical device safety : hearings before the Subcommittee on Health and the Environment of the Committee on Energy and Commerce, House of Representatives, One Hundred First Congress, on H.R. 3095 ... November 6, 1989 and July 17, 1990
Medical devices : FDA can improve oversight of tracking and recall systems : report to the Subcommittee on Oversight and Investigations, Committee on 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 Commerce, House of Representatives
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 : hearing before the Committee on Labor and Human Resources, United States Senate, One Hundred First Congress, second session, on examining proposed legislation to revise and strengthen the Food and Drug Administration's regulation of medical devices, July 25, 1990
Medical devices : protecting patients and promoting innovation : hearing of the Committee on Health, Education, Labor, and Pensions, United States Senate, One Hundred Twelfth Congress, first session ... November 15, 2011
Medical devices : protecting patients and promoting innovation : hearing of the Committee on Health, Education, Labor, and Pensions, United States Senate, One Hundred Twelfth Congress, first session ... November 15, 2011
Preamble compilation : Medical devices, March 1936-March 1978
Premarket notification, 510(k) : regulatory requirements for medical devices
Premarket notification--510(k) : regulatory requirements for medical devices
Programs affecting safety and innovation in pediatric therapies : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, first session, May 22, 2007
Public Law 94-295 : 94th Congress, S. 510, May 28, 1976 : an act to amend the Federal food, drug, and cosmetic act to provide for the safety and effectiveness of medical devices intended for human use, and for other purposes
Reprocessing of single-use medical devices : hearing of the Committee on Health, Education, Labor, and Pensions, United States Senate, One Hundred Sixth Congress, second session ... June 27, 2000
Safe Medical Devices Act of 1990 : conference report (to accompany H.R. 3095)
Safe Medical Devices Act of 1990 : report (to accompany H.R. 3095) (including cost estimate of the Congressional Budget Office)
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
Tools for compliance for the medical device and in vitrol diagnostic product industries

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Medical instruments and apparatus -- Safety regulations -- United States Resource Information The concept Medical instruments and apparatus -- Safety regulations -- United States represents the subject, aboutness, idea or notion of resources found in Indiana State Library.

47 Items that share the Concept Medical instruments and apparatus -- Safety regulations -- United States

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Medical instruments and apparatus -- Safety regulations -- United States

Resource Information

The concept Medical instruments and apparatus -- Safety regulations -- United States represents the subject, aboutness, idea or notion of resources found in Indiana State Library.