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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 23653340)

  • 1. Commentary: Europe needs a central, transparent, and evidence based regulation process for devices.
    Eikermann M; Gluud C; Perleth M; Wild C; Sauerland S; Gutierrez-Ibarluzea I; Antoine SL; Demotes-Mainard J; Neugebauer EA;
    BMJ; 2013 May; 346():f2771. PubMed ID: 23653340
    [No Abstract]   [Full Text] [Related]  

  • 2. 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; 81(12):1-6. PubMed ID: 33377827
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Standards for Medical Device Cybersecurity in 2018.
    Yuan S; Fernando A; Klonoff DC
    J Diabetes Sci Technol; 2018 Jul; 12(4):743-746. PubMed ID: 29575925
    [No Abstract]   [Full Text] [Related]  

  • 4. The FDA requires UDIs for medical devices. Now hospitals have to catch up.
    Rubenfire A; Conn J
    Mod Healthc; 2016 Sep; 46(38):16-18. PubMed ID: 30399296
    [No Abstract]   [Full Text] [Related]  

  • 5. European directives on medical devices.
    Ludgate SM; Potter DC
    BMJ; 1993 Aug; 307(6902):459-60. PubMed ID: 8400924
    [No Abstract]   [Full Text] [Related]  

  • 6. Assessing new developments in the pre-market regulatory process of medical devices in the People's Republic of China.
    Zhang S; Kriza C; Kolominsky-Rabas PL;
    Expert Rev Med Devices; 2014 Sep; 11(5):527-35. PubMed ID: 25060514
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Introduction of innovative high-risk medical devices in Europe: are clinical efficacy and safety guaranteed?].
    Stordeur S; Vinck I; Neyt M; Van Brabandt H; Hulstaert F
    Rev Epidemiol Sante Publique; 2013 Apr; 61(2):105-10. PubMed ID: 23477881
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Medical devices regulation needs to be overhauled, says cardiologist.
    Wise J
    BMJ; 2011 Oct; 343():d6671. PubMed ID: 22001786
    [No Abstract]   [Full Text] [Related]  

  • 9. The European legislation on medical devices.
    Anselmann N
    Stud Health Technol Inform; 1996; 28():5-12. PubMed ID: 10172825
    [TBL] [Abstract][Full Text] [Related]  

  • 10. How can we get high quality routine data to monitor the safety of devices and procedures?
    Campbell B; Stainthorpe AC; Longson CM
    BMJ; 2013 May; 346():f2782. PubMed ID: 23653341
    [No Abstract]   [Full Text] [Related]  

  • 11. How are medical devices regulated in the European Union?
    French-Mowat E; Burnett J
    J R Soc Med; 2012 Apr; 105 Suppl 1(Suppl 1):S22-8. PubMed ID: 22508970
    [No Abstract]   [Full Text] [Related]  

  • 12. CE marking and medical device directives.
    Shedden DJ
    Commun Dis Public Health; 1999 Jan; 2(1):73. PubMed ID: 10462905
    [No Abstract]   [Full Text] [Related]  

  • 13. A full-fledged overhaul is needed for a risk and value-based regulation of medical devices in Europe.
    Campillo-Artero C
    Health Policy; 2013 Nov; 113(1-2):38-44. PubMed ID: 23602548
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Comments on the interpretation of the term "medical devices"].
    Ferge Z
    Orv Hetil; 2013 Mar; 154(10):391-3. PubMed ID: 23461981
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Medical devices industry: the problem of clinical evaluation reports].
    Egbosimba D
    Ann Biol Clin (Paris); 2019 Oct; 77(5):514-516. PubMed ID: 31466939
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Certification of medical devices].
    Mashkov AV; Golikov VA
    Med Tekh; 2003; (1):51-3. PubMed ID: 12608074
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A study of medical device regulation management model in Asia.
    Wu YH; Li FA; Fan YT; Tu PW
    Expert Rev Med Devices; 2016 Jun; 13(6):533-43. PubMed ID: 27136699
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 29(4):284-92. PubMed ID: 7550495
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Bridging Unmet Medical Device Ecosystem Needs With Strategically Coordinated Registries Networks.
    Krucoff MW; Sedrakyan A; Normand SL
    JAMA; 2015 Oct; 314(16):1691-2. PubMed ID: 26302152
    [No Abstract]   [Full Text] [Related]  

  • 20. Patient groups accuse European parliament of putting economic interests ahead of safety on medical devices.
    Cohen D
    BMJ; 2013 Oct; 347():f6446. PubMed ID: 24157501
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.