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  1. 1
    Managing the risks from medical product use : creating a risk management framework : report to the FDA Commissioner from the Task Force on Risk Management.
    Published 1999
    Government Document Book
  2. 2
    Medical device register.
    Published 1981
    Serial
  3. 3
    FDA compliance program guidance manual /
    Published 1982
    Government Document Book
  4. 4
    Proceedings of the First International Conference of Medical Device Regulatory Authorities (ICMDRA), June 2-6, 1986 /
    Published 1987
    Government Document Conference Proceeding Book
  5. 5
    Reinventing drug and medical device regulation.
    Published 1995
    Get full text
    Government Document Book
  6. 6
    Food and Drug Administration : data to measure the timeliness of reviews of medical device applications are limited : report to congressional committees.
    Published 2004
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    Government Document eBook
  7. 7
    Performance report to Congress for the Medical Device User Fee and Modernization Act of 2002.
    Published 2003
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    Government Document Serial
  8. 8
    FY ... MDUFMA financial report required by the Medical Device User Fee and Modernization Act of 2002.
    Published 2003
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    Government Document Serial
  9. 9
    Global engagement /
    Published 2012
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    Government Document eBook
  10. 10
    Annual report of the medical devices annex to the U.S./EU mutual recognition agreement.
    Published 1999
    Get full text
    Government Document Serial
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