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PUBMED FOR HANDHELDS

Journal Abstract Search


297 related items for PubMed ID: 27890135

  • 1. Human factors in the design of medical devices - Approaches to meeting international standards in the European Union and USA.
    Privitera MB, Evans M, Southee D.
    Appl Ergon; 2017 Mar; 59(Pt A):251-263. PubMed ID: 27890135
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  • 2. Designing medical devices for conformance with harmonized standards. The European Community's Medical Devices Directives and their effect on the product development process.
    Fries RC, Graber MD.
    Biomed Instrum Technol; 1995 Mar; 29(4):284-92. PubMed ID: 7550495
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  • 8. The European legislation on medical devices.
    Anselmann N.
    Stud Health Technol Inform; 1996 Mar; 28():5-12. PubMed ID: 10172825
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  • 9. Medical Device Regulation: A Comparison of the United States and the European Union.
    Maak TG, Wylie JD.
    J Am Acad Orthop Surg; 2016 Aug; 24(8):537-43. PubMed ID: 27195383
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  • 12. The greening of standards.
    Moore R.
    Med Device Technol; 2003 Oct; 14(8):28. PubMed ID: 14603717
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  • 13. FDA recognition of consensus standards in the premarket notification program.
    Marlowe DE, Phillips PJ.
    Biomed Instrum Technol; 1998 Oct; 32(3):301-4. PubMed ID: 9619259
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  • 14. [The Suggestion of Introducing the 3rd Party Review System by Reference of EU New Medical Device Regulations].
    Li Y, Fan Y.
    Zhongguo Yi Liao Qi Xie Za Zhi; 2017 Nov 30; 41(6):440-442. PubMed ID: 29862706
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  • 16. Medical device development: the challenge for ergonomics.
    Martin JL, Norris BJ, Murphy E, Crowe JA.
    Appl Ergon; 2008 May 30; 39(3):271-83. PubMed ID: 18061139
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  • 20. Self-preservation in the face of regulatory adversity.
    Sheridan B.
    Med Device Technol; 2001 May 30; 12(1):43-5. PubMed ID: 11317866
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