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 *

254 related articles for article (PubMed ID: 19436959)

  • 1. [Medical devices and patient safety from the clinicians' view].
    Mellert F; Mallek D
    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2009 Jun; 52(6):584-8. PubMed ID: 19436959
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Relevancy and binding character of standards for the safety of medical devices].
    Rölleke T
    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2009 Jun; 52(6):605-9. PubMed ID: 19399374
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Information on the policies of the Medical Devices Safety Act].
    Wetzel D; von Mallek D
    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2009 Jun; 52(6):577-8. PubMed ID: 19407937
    [No Abstract]   [Full Text] [Related]  

  • 4. [Safety of medical devices].
    Broich K; Lauer W
    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2014 Dec; 57(12):1353-4. PubMed ID: 25394355
    [No Abstract]   [Full Text] [Related]  

  • 5. [Arthroplasty registries and their contribution to the safety of patient care in joint replacement].
    Heinz BC
    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2009 Jun; 52(6):589-93. PubMed ID: 19412594
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Medical devices. Regulatory framework and contribution of the German Federal Institute for Drugs and Medical Devices (BfArM) to the safe application].
    Lauer W; Stößlein E; Brinker A; Broich K
    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2014 Dec; 57(12):1355-61. PubMed ID: 25370170
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Safety of high risk in vitro diagnostic medical devices : international and national measures].
    Halbauer J; Siekmeier R; Funk M
    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2009 Jun; 52(6):610-8. PubMed ID: 19421725
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [The global harmonization task force : successes and challenges].
    Rotter RG
    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2009 Jun; 52(6):601-4. PubMed ID: 19418030
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Global harmonization--a catalyst for safety.
    Jacques T
    Occup Health Saf; 2010 May; 79(5):48-9. PubMed ID: 20491303
    [No Abstract]   [Full Text] [Related]  

  • 11. Medical device epidemiology and surveillance: patient safety is the bottom line.
    Brown SL; Bright RA; Tavris DR
    Expert Rev Med Devices; 2004 Sep; 1(1):1-2. PubMed ID: 16293003
    [No Abstract]   [Full Text] [Related]  

  • 12. [Experiences and recommendations of the German Federal Institute for Drugs and Medical Devices (BfArM) concerning clinical investigation of medical devices and the evaluation of serious adverse events (SAE)].
    Renisch B; Lauer W
    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2014 Dec; 57(12):1368-75. PubMed ID: 25376539
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Medical devices; illustrative and designated lists for device tracking--FDA. Final rule and request for comments.
    Fed Regist; 1993 Aug; 58(156):43451-5. PubMed ID: 10171508
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Prevention of medical device-related adverse events in hospitals: Specifying the recommendations of the German Coalition for Patient Safety (APS) for users and operators of anaesthesia equipment].
    Bohnet-Joschko S; Zippel C; Siebert H
    Z Evid Fortbild Qual Gesundhwes; 2015; 109(9-10):725-35. PubMed ID: 26699261
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ensuring safe and effective medical devices.
    Feigal DW; Gardner SN; McClellan M
    N Engl J Med; 2003 Jan; 348(3):191-2. PubMed ID: 12529457
    [No Abstract]   [Full Text] [Related]  

  • 16. [Focus Notified Bodies. New requirements for designation and monitoring].
    Poos U; Edelhäuser R
    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2014 Dec; 57(12):1362-7. PubMed ID: 25373553
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Medical devices; device tracking--FDA. Final rule; suspension of effective date; notification of status under the Safe Medical Devices Act; technical amendments.
    Fed Regist; 1993 Aug; 58(156):43442-51. PubMed ID: 10127886
    [TBL] [Abstract][Full Text] [Related]  

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

  • 19. German law: the differences.
    Müller-Lierheim WG
    Med Device Technol; 1997 Nov; 8(9):38-40. PubMed ID: 10174630
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Medical devices; medical device distributor reporting; opportunity for comments--FDA. Final rule; opportunity for comments.
    Fed Regist; 1993 Sep; 58(168):46514. PubMed ID: 10128334
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.