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Medical Instruments And Apparatus Industry Law And Legislation United States
1
E-Book/E-Doc
 

Discussion drafts concerning Prescription Drug User Fee Act reauthorization, Medical Device User Fee


United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health.
Washington : U.S. G.P.O. : For sale by the Supt. of Docs., U.S. G.P.O., 2008. 2008

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 Axe Federal Documents Online  Y 4.C 73/8:110-55    ---  Available
2
E-Book/E-Doc
 

The FDA and worldwide quality system requirements guidebook for medical devices



Milwaukee, Wisconsin : ASQ Quality Press, 2008. 2008

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 Axe ProQuest E-Book  Electronic Book    ---  Available
3
Print Material
 

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


Thaul, Susan, author.
[Washington, D.C.] : Congressional Research Service, 2018- 2018

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4
E-Book/E-Doc
 

Reauthorization of MDUFA what it means for jobs, innovation, and patients : hearing before the Subco


United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health, author.
Washington : U.S. Government Printing Office, 2012. 2012

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Location Call No. OPAC Message Status
 Axe Federal Documents Online  Y 4.C 73/8:112-116    ---  Available
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