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  1. 1
    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 /
    by Crosse, Marcia
    Published 2009
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  2. 2
    Medical devices status of FDA's program for inspections by accredited organizations : report to congressional committees.
    Published 2007
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  3. 3
    Cost-contained regulatory compliance : for the pharmaceutical, biologics, and medical device industries /
    by Weinberg, Sandy, 1950-
    Published 2011
    Available to Lehigh users via EBSCO
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    Available to Lehigh users via Wiley Online Library
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  4. 4
    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 /
    by Crosse, Marcia
    Published 2008
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