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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

516 related items for PubMed ID: 12938545

  • 21. EU and US clinical investigation adverse event reporting.
    Crowley G.
    Med Device Technol; 2004 Jun; 15(5):30-2. PubMed ID: 15285486
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  • 22. Managing clinical data for worldwide acceptance.
    Donawa M.
    Med Device Technol; 2006 Oct; 17(8):26-8. PubMed ID: 17153369
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  • 26. Activities in other European countries.
    Ecker W, De Roo R, Frellsen M, Gomes AF, Gutowski R.
    Stud Health Technol Inform; 1996 Oct; 28():119-23. PubMed ID: 10164088
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  • 27. Avoiding loss of medical information during clinical investigations.
    Gruber R.
    Med Device Technol; 2005 Mar; 16(2):22-4. PubMed ID: 15828496
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  • 29. Ireland's competent authority initiatives.
    Scully C.
    Stud Health Technol Inform; 1996 Mar; 28():101-11. PubMed ID: 10164084
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  • 30. Risk management of European device clinical studies.
    Donawa M.
    Med Device Technol; 2007 Mar; 18(2):39-42. PubMed ID: 17494500
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  • 34. Standards update.
    Moore R.
    Med Device Technol; 2003 Mar; 14(1):36. PubMed ID: 12974124
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  • 35. Medical device problem reporting for the betterment of healthcare.
    Health Devices; 1998 Aug; 27(8):277-92. PubMed ID: 9743900
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  • 36. Medical device accident reporting: does it improve patient safety?
    Nobel JJ.
    Stud Health Technol Inform; 1996 Aug; 28():29-35. PubMed ID: 10172828
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  • 38. The dilemma of reporting device-related adverse events.
    Donawa M.
    Med Device Technol; 2003 Aug; 14(1):26-31. PubMed ID: 12974122
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