These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

182 related items for PubMed ID: 17969510

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. Validation and Six Sigma.
    Barry E.
    Med Device Technol; 2008; 19(7):36, 38-40. PubMed ID: 19133627
    [Abstract] [Full Text] [Related]

  • 4. Effectively incorporating risk management into quality systems.
    Donawa M.
    Med Device Technol; 2006 Jun; 17(5):28-30. PubMed ID: 16903387
    [Abstract] [Full Text] [Related]

  • 5. Safe Medical Devices Act: management guidance for hospital compliance with the new FDA requirements.
    Alder HC.
    Hosp Technol Ser; 1993 Oct; 12(11):1-27. PubMed ID: 10129209
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Managing equipment failures: nursing practice requirements for meeting the challenges of the Safe Medical Devices Act.
    Cuthrell P.
    J Intraven Nurs; 1996 Oct; 19(5):264-8. PubMed ID: 9060352
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Medical devices; current good manufacturing practice (CGMP) final fule; quality system regulation--FDA. Final rule.
    Fed Regist; 1996 Oct 07; 61(195):52602-62. PubMed ID: 10168287
    [Abstract] [Full Text] [Related]

  • 10. ISO 9000:2000 revisions and their implications.
    Sim P.
    Med Device Technol; 2000 May 07; 11(4):45-7. PubMed ID: 11010320
    [Abstract] [Full Text] [Related]

  • 11. Risk management of European device clinical studies.
    Donawa M.
    Med Device Technol; 2007 May 07; 18(2):39-42. PubMed ID: 17494500
    [Abstract] [Full Text] [Related]

  • 12. Final FDA inspection manual.
    Donawa M.
    Med Device Technol; 2001 Apr 07; 12(3):29-32. PubMed ID: 11547684
    [Abstract] [Full Text] [Related]

  • 13. [Discussion about the application of risk management to medical devices].
    Xu FL.
    Zhongguo Yi Liao Qi Xie Za Zhi; 2006 Mar 07; 30(2):123-8. PubMed ID: 16830807
    [Abstract] [Full Text] [Related]

  • 14. Conducting clinical studies in Italy.
    Donawa M.
    Med Device Technol; 2005 Oct 07; 16(8):21-4. PubMed ID: 16355966
    [Abstract] [Full Text] [Related]

  • 15. Controlling the quality of raw materials.
    Donawa ME.
    Med Device Technol; 1998 Oct 07; 9(1):12-5. PubMed ID: 10176139
    [Abstract] [Full Text] [Related]

  • 16. Update on the European database.
    Donawa M.
    Med Device Technol; 2001 Oct 07; 12(8):21-4. PubMed ID: 12938545
    [Abstract] [Full Text] [Related]

  • 17. Medical device problem reporting for the betterment of healthcare.
    Health Devices; 1998 Aug 07; 27(8):277-92. PubMed ID: 9743900
    [Abstract] [Full Text] [Related]

  • 18. [Research on quality system management of software manufacturers for medical devices].
    Zheng JG, Xu YN.
    Zhongguo Yi Liao Qi Xie Za Zhi; 2005 Jul 07; 29(4):292-4. PubMed ID: 16268361
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. [How to apply for european CE certification for Chinese medical device manufacturers].
    Xu XG.
    Zhongguo Yi Liao Qi Xie Za Zhi; 2006 Nov 07; 30(6):453-6. PubMed ID: 17300018
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.