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Journal Abstract Search

270 related items for PubMed ID: 29862706

  • 1. [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
    [Abstract] [Full Text] [Related]

  • 2. [Simple Suggestion of Adapting Requirements of Medical Devices New Supervision Regulation System for Medical Device Manufacturers].
    Li Y, Chu Z, Fan Y.
    Zhongguo Yi Liao Qi Xie Za Zhi; 2017 May 30; 41(3):220-223. PubMed ID: 29862773
    [Abstract] [Full Text] [Related]

  • 3. A study of medical device regulation management model in Asia.
    Wu YH, Li FA, Fan YT, Tu PW.
    Expert Rev Med Devices; 2016 Jun 30; 13(6):533-43. PubMed ID: 27136699
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  • 4. The impact of medical device regulation on hospital doctors who prescribe and manufacture custom-made devices.
    Green JI.
    Br J Hosp Med (Lond); 2020 Dec 02; 81(12):1-6. PubMed ID: 33377827
    [Abstract] [Full Text] [Related]

  • 5. [Analysis of Changes in Medical Device Classification Concept of the New EU Regulations].
    Zhang C, Zhou L, Wang Y, Yi L, Yang W, Rong S, Li J.
    Zhongguo Yi Liao Qi Xie Za Zhi; 2018 May 30; 42(3):202-205. PubMed ID: 29885129
    [Abstract] [Full Text] [Related]

  • 6. Legal regulation of the production and trade of medical devices and medical equipment in the EU and US: experience for Ukraine.
    Pashkov V, Kotvitska A, Harkusha A.
    Wiad Lek; 2017 May 30; 70(3 pt 2):614-618. PubMed ID: 28713093
    [Abstract] [Full Text] [Related]

  • 7. Medical Device Regulation: Requirements for Dental Professionals Who Prescribe and Manufacture Custom-Made Devices.
    Green JIJ.
    Prim Dent J; 2021 Mar 30; 10(1):64-88. PubMed ID: 33722134
    [Abstract] [Full Text] [Related]

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  • 10. Medical Device Regulations and custom-made device documentation: Ten frequently asked questions and their answers.
    Green JIJ.
    Prim Dent J; 2022 Jun 30; 11(2):22-31. PubMed ID: 35658659
    [Abstract] [Full Text] [Related]

  • 11. Regulatory convergence of medical devices: a case study using ISO and IEC standards.
    Imagawa K, Mizukami Y, Miyazaki S.
    Expert Rev Med Devices; 2018 Jul 30; 15(7):497-504. PubMed ID: 29936871
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  • 12. 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 30; 59(Pt A):251-263. PubMed ID: 27890135
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  • 13. Neither protective nor harmonized: the crossborder regulation of medical devices in the EU.
    Jarman H, Rozenblum S, Huang TJ.
    Health Econ Policy Law; 2021 Jan 30; 16(1):51-63. PubMed ID: 32631465
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  • 16. [How to apply for european CE certification for Chinese medical device manufacturers].
    Xu XG.
    Zhongguo Yi Liao Qi Xie Za Zhi; 2006 Nov 30; 30(6):453-6. PubMed ID: 17300018
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  • 17. Medical device regulation for manufacturers.
    McAllister P, Jeswiet J.
    Proc Inst Mech Eng H; 2003 Nov 30; 217(6):459-67. PubMed ID: 14702983
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