BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

115 related articles for article (PubMed ID: 12534163)

  • 1. Tagging medical devices.
    Med Device Technol; 2002 Nov; 13(9):76-7. PubMed ID: 12534163
    [No Abstract]   [Full Text] [Related]  

  • 2. Medical device accident reporting: does it improve patient safety?
    Nobel JJ
    Stud Health Technol Inform; 1996; 28():29-35. PubMed ID: 10172828
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Assessment of service life of sophisticated medical equipment].
    Toporkov AA
    Med Tekh; 2007; (3):26-33. PubMed ID: 17598479
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Need for a National Evaluation System for Health Technology.
    Shuren J; Califf RM
    JAMA; 2016 Sep; 316(11):1153-4. PubMed ID: 27398696
    [No Abstract]   [Full Text] [Related]  

  • 5. Pharmaceuticals and medical devices: medical devices.
    ; Berry MD
    Issue Brief Health Policy Track Serv; 2012 Jan; ():1-38. PubMed ID: 22403842
    [No Abstract]   [Full Text] [Related]  

  • 6. Pharmaceuticals and medical devices: medical devices.
    Berry MD
    Issue Brief Health Policy Track Serv; 2013 Dec; ():1-49. PubMed ID: 24482892
    [No Abstract]   [Full Text] [Related]  

  • 7. Surveillance of medical technologies.
    Thacker SB; Berkelman RL
    J Public Health Policy; 1986; 7(3):363-77. PubMed ID: 3771786
    [No Abstract]   [Full Text] [Related]  

  • 8. EU agrees tighter standards for medical devices.
    Watson R
    BMJ; 2016 Jun; 353():i3058. PubMed ID: 27251309
    [No Abstract]   [Full Text] [Related]  

  • 9. Postmarket surveillance for medical devices: America's new strategy.
    Normand SL; Hatfield L; Drozda J; Resnic FS
    BMJ; 2012 Oct; 345():e6848. PubMed ID: 23060660
    [No Abstract]   [Full Text] [Related]  

  • 10. New medical devices reporting requirements.
    Carley MM
    Contemp Longterm Care; 1991 Dec; 14(12):66, 68. PubMed ID: 10117951
    [No Abstract]   [Full Text] [Related]  

  • 11. Millions to benefit from the Safe Medical Devices Act (SMDA) of 1990.
    Nichols DG
    J AHIMA; 1992 Feb; 63(2):60-2. PubMed ID: 10171005
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. Advances in the Use of Real-World Evidence for Medical Devices: An Update From the National Evaluation System for Health Technology.
    Fleurence RL; Shuren J
    Clin Pharmacol Ther; 2019 Jul; 106(1):30-33. PubMed ID: 30888048
    [No Abstract]   [Full Text] [Related]  

  • 14. Blowing the whistle on faulty medical products.
    Harris HR
    Surg Technol; 1993 Aug; 25(8):13, 18. PubMed ID: 10127818
    [No Abstract]   [Full Text] [Related]  

  • 15. Generating change. Health Devices motivates suppliers to improve their products.
    Health Devices; 2001 Jun; 30(6):197-9. PubMed ID: 11447864
    [No Abstract]   [Full Text] [Related]  

  • 16. Safe Medical Devices Act of 1990: current hospital requirements and recommended actions.
    Alder H
    Healthc Facil Manag Ser; 1993 Sep; ():1-34. PubMed ID: 10132639
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Post-marketing device safety surveillance.
    Vidi VD; Matheny ME; Resnic FS
    Contemp Clin Trials; 2011 May; 32(3):307-8. PubMed ID: 21371573
    [No Abstract]   [Full Text] [Related]  

  • 18. MedWatch. On lookout for medical product problems.
    Ropp KL
    FDA Consum; 1993 Nov; 27(9):14-7. PubMed ID: 10130376
    [No Abstract]   [Full Text] [Related]  

  • 19. Medical device incident investigation.
    Baretich MF
    Biomed Sci Instrum; 2007; 43():302-5. PubMed ID: 17487098
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Standardize and synchronize product data for safety.
    Perry R
    Hosp Mater Manage; 2007 May; 32(5):2. PubMed ID: 17526398
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.