Subject: "Medical instruments and apparatus" / Genre: Rules and practice

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Medical devices : European Union's regulatory process
by United States. General Accounting Office. Health, Education, and Human Services Division
1997
Format: Book and Microform

✔ Available Joyner - Microforms B300

Call Number: GA 1.13:HEHS-98-19 R

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
2017
Format: Electronic and Book

✔ Available

Call Number: Access Content Online

✔ Available

Call Number: Access Content Online

Medical devices : challenges for FDA in conducting manufacturer inspections : testimony before the Subcommittee on Oversight and Investigations, Committee on Energy and Commerce, House of Representatives
by Crosse, Marcia
2008
Format: Electronic and Book

✔ Available

Call Number: Access Content Online

✔ Available

Call Number: Access Content Online

Medicare : impact of changing transportation policy for portable equipment is uncertain : report to congressional requesters
by United States. General Accounting Office
1998
Format: Book and Microform

✔ Available Joyner - Microforms B300

Call Number: GA 1.13:HEHS-98-82

✔ Available Joyner - Fed Docs Stacks

Call Number: Y 4.V 64/3:113-49

Durable medical equipment regional carriers : meeting HCFA's objectives
by United States. Department of Health and Human Services. Office of Inspector General
2000
Format: Electronic and Book

✔ Available

Call Number: Access Content Online

FDA user fees and the regulation of drugs, biologics, and devices : comparative analysis of S. 3187 and H.R. 5651
by Thaul, Susan
2018
Format: Electronic and Book

✔ Available

Call Number: Access Content Online

✔ Available

Call Number: Access Content Online

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Medical devices : European Union's regulatory process

FDA medical device reviews, evaluation is needed to assure requests for additional information follow a least burdensome approach : report to congressional requesters

Medical devices : shortcomings in FDA's premarket review, postmarket surveillance, and inspections of device manufacturing establishments : testimony before the Subcommittee on Health, Committee on Energy and Commerce, House of Representatives

Medical devices : challenges for FDA in conducting manufacturer inspections : testimony before the Subcommittee on Oversight and Investigations, Committee on Energy and Commerce, House of Representatives

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

Medicare : impact of changing transportation policy for portable equipment is uncertain : report to congressional requesters

Vendors in the OR : VA's failed oversight of surgical implants : hearing before the Subcommittee on Oversight and Investigations of the Committee on Veterans' Affairs, U.S. House of Representatives, One Hundred Thirteenth Congress, second session, Wednesday, January 15, 2014

Durable medical equipment regional carriers : meeting HCFA's objectives

FDA user fees and the regulation of drugs, biologics, and devices : comparative analysis of S. 3187 and H.R. 5651

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