Medical instruments and apparatus industry -- Government policy -- United States

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The concept Medical instruments and apparatus industry -- Government policy -- United States represents the subject, aboutness, idea or notion of resources found in Boston University Libraries.

The Resource Medical instruments and apparatus industry -- Government policy -- United States

Label: Medical instruments and apparatus industry -- Government policy -- United States

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Medical instruments and apparatus industry

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Government policy
United States

6 Items that share the Concept Medical instruments and apparatus industry -- Government policy -- United States

CMS regulation of healthcare services : hearing before the Committee on Small Business, House of Representatives, One Hundred Seventh Congress, second session, Washington, DC, October 3, 2002

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Food and Drug Administration : methodologies for identifying and allocating costs of reviewing medical device applications are consistent with federal cost accounting standards, and staffing levels for reviews have generally increased in recent years

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Medicare : CMS has addressed some implementation problems from round 1 of the Durable Medical Equipment competitive bidding program for the round 1 rebid : testimony before the Subcommittee on Health, Committee on Energy and Commerce, House of Representatives, statement of Kathleen M. King., (electronic resource :)

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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

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Role of commissioner of food and drugs : hearing before the Committee on Labor and Human Resources, United States Senate, One Hundred Second Congress, first session, on examining the role of the current commissioner of the Food and Drug Administration, March 6, 1991

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Context of Medical instruments and apparatus industry -- Government policy -- United States

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CMS regulation of healthcare services : hearing before the Committee on Small Business, House of Representatives, One Hundred Seventh Congress, second session, Washington, DC, October 3, 2002
Food and Drug Administration : methodologies for identifying and allocating costs of reviewing medical device applications are consistent with federal cost accounting standards, and staffing levels for reviews have generally increased in recent years
Food and Drug Administration : methodologies for identifying and allocating costs of reviewing medical device applications are consistent with federal cost accounting standards, and staffing levels for reviews have generally increased in recent years.
Medicare : CMS has addressed some implementation problems from round 1 of the Durable Medical Equipment competitive bidding program for the round 1 rebid : testimony before the Subcommittee on Health, Committee on Energy and Commerce, House of Representatives
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
Role of commissioner of food and drugs : hearing before the Committee on Labor and Human Resources, United States Senate, One Hundred Second Congress, first session, on examining the role of the current commissioner of the Food and Drug Administration, March 6, 1991

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Medical instruments and apparatus industry -- Government policy -- United States

Resource Information

The concept Medical instruments and apparatus industry -- Government policy -- United States represents the subject, aboutness, idea or notion of resources found in Boston University Libraries.

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