Medical device reporting : improvements needed in FDA's system for monitoring problems with approved devices : report to Congressional committees /

Drug regulation : FDA's computer systems need to be better managed : report to the Chairman, Subcommittee on Intergovernmental Relations and Human Resources, Committee on Government Operations, House of Representatives /

United States. General Accounting Office.

"B-223076"--P. [1]."GAO/IMTEC-86-32.""September 1986."Distributed to depository libraries in microfi...

Medical Device Regulatory Modernization Act of 1997 : report, together with additional views (to accompany H.R. 1710) (including cost estimate of the Congressional Budget Office).

United States. Congress. House. Committee on Commerce.

"October 6, 1997."Shipping list no.: 98-0034-P.Distributed to some depository libraries in microfich...

Regulating innovation : FDA's medical device approval process : hearing before the Subcommittee on Investigations and Oversight of the Committee on Science, Space, and Technology, U.S. House of Representatives, One Hundred Third Congress, first session, September 17, 1993.

United States. Congress. House. Committee on Science, Space, and Technology. Subcommittee on Investigations and Oversight.

"No. 69."Shipping list no.: 94-0020-P.Distributed to some depository libraries in microfiche.Mode of...

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.
United States. Congress. House. Committee on Commerce. Subcommittee on Oversight and Investigations.

"September 1998"GAO/HEHS-98-211."Cover title.Includes bibliographical references.Mode of access: Int...

Medical devices : FDA's implementation of the medical device reporting regulation : report to the Chairman, Subcommittee on Health and the Environment, Committee on Energy and Commerce, House of Representatives /

United States. General Accounting Office.
United States. Congress. Committee on Energy and Commerce. Subcommittee on Health and the Environment.

January 1989

"B-223710"--p.[1]"GAO/PEMD-89-10""February 1989"Cover title."References": p.83.Mode of access: Inter...

Medical devices : FDA review time : report to the Chairman, Subcommittee on Oversight and Investigations, Committee on Commerce, House of Representatives /

United States. General Accounting Office.
United States. Congress. House. Committee on Commerce. Subcommittee on Oversight and Investigations.

"B-261822"--P. 1."GAO/PEMD-96-2.""October 1995."Cover title.Includes bibliographical references.Mode...

Medical devices : FDA's forecasts of problem reports and FTEs under H.R. 4640 : report to the Chairman, Subcommittee on Health and the Environment, Committee on Energy and Commerce, House of Representatives /

United States. General Accounting Office.
United States. Congress. Committee on Energy and Commerce. Subcommittee on Health and the Environment.

"B-231242"--p.1."GAO/PEMD-88-30""July 1988"Cover title.Includes bibliographical references.Mode of a...

Medical devices : FDA's 510(k) operations could be improved : report to the chairman, Subcommittee on Health and the Environment, Committee on Energy and Commerce, House of Representative /

United States. General Accounting Office.
United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health and the Environment.

"B-229400"--p. [1]"GAO/PEMD-88-14""August 1988"Running title: FDA's implementation of premarket noti...

FDA's mammography inspections : while some problems need attention, facility compliance is growing : report to Congressional committees /

United States. General Accounting Office.

"B-271339"--P. 1."GAO/HEHS-97-25.""January 1997."Cover title.Includes bibliographical references.Mod...

Medical devices : early warning of problems is hampered by severe underreporting : report to the chairman, Committee on Governmental Affairs, United States Senate.

United States. General Accounting Office.
United States. Congress. Senate. Committee on Governmental Affairs.

"GA0/PEMD-87-1.""December 1986."Cover title.Bibliography: p. 119-126.Mode of access: Internet

Drug safety : improvement needed in FDA's postmarket decision-making and oversight process : report to Congressional requesters.

United States. Government Accountability Office.

"GAO-06-402.""March 2006."Cover title.Includes bibliographical references.Mode of access: Internet

FDA and the medical device industry : hearing before the Subcommittee on Oversight and Investigations of the Committee on Energy and Commerce, House of Representatives, One Hundred First Congress, second session, February 26, 1990.

United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Oversight and Investigations.

January 1990

"Serial no. 101-127."Includes bibliographical references.Mode of access: Internet

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.
United States. Congress. Senate. Committee on Labor and Human Resources.

"B-260738"--P. 1."GAO/HEHS-96-65.""March 1996."Cover title.Includes bibliographical references (p. 4...

FDA drug approval : review time has decreased in recent years : report to Congressional requesters /

United States. General Accounting Office.

"B-266023"--P. 1."GAO/PEMD-96-1.""October 1995."Cover title.Includes bibliographical references.Mode...

Medical devices : underreporting of serious problems with a home apnea monitor : report to the Chairman, Subcommittee on Health and the Environment, Committee on Energy and Commerce, House of Representatives /

United States. General Accounting Office.
United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health and the Environment.

January 1990

"B-237533"--p. 1."May 1990"Cover title."GAO/PEMD-90-17""Related GAO products": p.40.Mode of access: ...

Drug regulation : FDA's computer systems need to be better managed : report to the Chairman, Subcommittee on Intergovernmental Relations and Human Resources, Committee on Government Operations, House of Representatives /

United States. General Accounting Office.

"B-223076"--P. [1]."GAO/IMTEC-86-32.""September 1986."Distributed to depository libraries in microfi...

Medical Device Regulatory Modernization Act of 1997 : report, together with additional views (to accompany H.R. 1710) (including cost estimate of the Congressional Budget Office).

United States. Congress. House. Committee on Commerce.

"October 6, 1997."Shipping list no.: 98-0034-P.Distributed to some depository libraries in microfich...

Regulating innovation : FDA's medical device approval process : hearing before the Subcommittee on Investigations and Oversight of the Committee on Science, Space, and Technology, U.S. House of Representatives, One Hundred Third Congress, first session, September 17, 1993.

United States. Congress. House. Committee on Science, Space, and Technology. Subcommittee on Investigations and Oversight.

"No. 69."Shipping list no.: 94-0020-P.Distributed to some depository libraries in microfiche.Mode of...

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.
United States. Congress. House. Committee on Commerce. Subcommittee on Oversight and Investigations.

"September 1998"GAO/HEHS-98-211."Cover title.Includes bibliographical references.Mode of access: Int...

Medical devices : FDA's implementation of the medical device reporting regulation : report to the Chairman, Subcommittee on Health and the Environment, Committee on Energy and Commerce, House of Representatives /

United States. General Accounting Office.
United States. Congress. Committee on Energy and Commerce. Subcommittee on Health and the Environment.

January 1989

"B-223710"--p.[1]"GAO/PEMD-89-10""February 1989"Cover title."References": p.83.Mode of access: Inter...

Medical devices : FDA review time : report to the Chairman, Subcommittee on Oversight and Investigations, Committee on Commerce, House of Representatives /

United States. General Accounting Office.
United States. Congress. House. Committee on Commerce. Subcommittee on Oversight and Investigations.

"B-261822"--P. 1."GAO/PEMD-96-2.""October 1995."Cover title.Includes bibliographical references.Mode...

Medical devices : FDA's forecasts of problem reports and FTEs under H.R. 4640 : report to the Chairman, Subcommittee on Health and the Environment, Committee on Energy and Commerce, House of Representatives /

United States. General Accounting Office.
United States. Congress. Committee on Energy and Commerce. Subcommittee on Health and the Environment.

"B-231242"--p.1."GAO/PEMD-88-30""July 1988"Cover title.Includes bibliographical references.Mode of a...

Medical devices : FDA's 510(k) operations could be improved : report to the chairman, Subcommittee on Health and the Environment, Committee on Energy and Commerce, House of Representative /

United States. General Accounting Office.
United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health and the Environment.

"B-229400"--p. [1]"GAO/PEMD-88-14""August 1988"Running title: FDA's implementation of premarket noti...

FDA's mammography inspections : while some problems need attention, facility compliance is growing : report to Congressional committees /

United States. General Accounting Office.

"B-271339"--P. 1."GAO/HEHS-97-25.""January 1997."Cover title.Includes bibliographical references.Mod...

Medical devices : early warning of problems is hampered by severe underreporting : report to the chairman, Committee on Governmental Affairs, United States Senate.

United States. General Accounting Office.
United States. Congress. Senate. Committee on Governmental Affairs.

"GA0/PEMD-87-1.""December 1986."Cover title.Bibliography: p. 119-126.Mode of access: Internet

Drug safety : improvement needed in FDA's postmarket decision-making and oversight process : report to Congressional requesters.

United States. Government Accountability Office.

"GAO-06-402.""March 2006."Cover title.Includes bibliographical references.Mode of access: Internet

FDA and the medical device industry : hearing before the Subcommittee on Oversight and Investigations of the Committee on Energy and Commerce, House of Representatives, One Hundred First Congress, second session, February 26, 1990.

United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Oversight and Investigations.

January 1990

"Serial no. 101-127."Includes bibliographical references.Mode of access: Internet

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.
United States. Congress. Senate. Committee on Labor and Human Resources.

"B-260738"--P. 1."GAO/HEHS-96-65.""March 1996."Cover title.Includes bibliographical references (p. 4...

FDA drug approval : review time has decreased in recent years : report to Congressional requesters /

United States. General Accounting Office.

"B-266023"--P. 1."GAO/PEMD-96-1.""October 1995."Cover title.Includes bibliographical references.Mode...

Medical devices : underreporting of serious problems with a home apnea monitor : report to the Chairman, Subcommittee on Health and the Environment, Committee on Energy and Commerce, House of Representatives /

United States. General Accounting Office.
United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health and the Environment.

January 1990

"B-237533"--p. 1."May 1990"Cover title."GAO/PEMD-90-17""Related GAO products": p.40.Mode of access: ...

Drug regulation : FDA's computer systems need to be better managed : report to the Chairman, Subcommittee on Intergovernmental Relations and Human Resources, Committee on Government Operations, House of Representatives /

United States. General Accounting Office.

"B-223076"--P. [1]."GAO/IMTEC-86-32.""September 1986."Distributed to depository libraries in microfi...

Medical Device Regulatory Modernization Act of 1997 : report, together with additional views (to accompany H.R. 1710) (including cost estimate of the Congressional Budget Office).

United States. Congress. House. Committee on Commerce.

"October 6, 1997."Shipping list no.: 98-0034-P.Distributed to some depository libraries in microfich...

Regulating innovation : FDA's medical device approval process : hearing before the Subcommittee on Investigations and Oversight of the Committee on Science, Space, and Technology, U.S. House of Representatives, One Hundred Third Congress, first session, September 17, 1993.

United States. Congress. House. Committee on Science, Space, and Technology. Subcommittee on Investigations and Oversight.

"No. 69."Shipping list no.: 94-0020-P.Distributed to some depository libraries in microfiche.Mode of...

Medical device reporting : improvements needed in FDA's system for monitoring problems with approved devices : report to Congressional committees /

Abstract

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Medical device reporting : improvements needed in FDA's system for monitoring problems with approved devices : report to Congressional committees /

Abstract

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