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 *

101 related articles for article (PubMed ID: 22428654)

  • 21. European medical device regulation: a new era?
    Donawa M
    Med Device Technol; 2004 Dec; 15(10):30-1. PubMed ID: 16225282
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Clinical investigations with medical devices. New rules.
    Kennedy RS
    JAMA; 1981 May 22-29; 245(20):2052-5. PubMed ID: 7230401
    [No Abstract]   [Full Text] [Related]  

  • 23. AAMI releases new guidance for software validation.
    Bremner J
    Biomed Instrum Technol; 2008; 42(2):149. PubMed ID: 18397139
    [No Abstract]   [Full Text] [Related]  

  • 24. Codes and standards.
    Soltys M
    Biomed Instrum Technol; 1990; 24(2):141-3. PubMed ID: 2322759
    [No Abstract]   [Full Text] [Related]  

  • 25. Eight steps to integrating security standards.
    Happ J;
    Biomed Instrum Technol; 2006; Suppl():22-4. PubMed ID: 16596845
    [No Abstract]   [Full Text] [Related]  

  • 26. Notified Body guidance on clinical evaluation.
    Donawa M
    Med Device Technol; 2000 Sep; 11(7):26-8. PubMed ID: 15326742
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Voluntary standards: development and use.
    Miller MJ
    Med Instrum; 1979; 13(4):203-6. PubMed ID: 470660
    [No Abstract]   [Full Text] [Related]  

  • 28. To Be or not to Be a Medical Device: Is the Regulatory Framework a Safety Rope or a Fetter?
    Röhrig R
    Methods Inf Med; 2015; 54(3):291-2. PubMed ID: 25894838
    [No Abstract]   [Full Text] [Related]  

  • 29. Proposed amendments to the medical devices Directives.
    Donawa M
    Med Device Technol; 2006; 17(1):22-5. PubMed ID: 16483107
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Software as a medical device: regulatory critical issues.
    Pelayo S; Bras Da Costa S; Leroy N; Loiseau S; Beuscart-Zephir MC
    Stud Health Technol Inform; 2013; 183():337-42. PubMed ID: 23388310
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A systems approach to standards development.
    Hammer GS
    Med Instrum; 1977; 11(4):250-1. PubMed ID: 895600
    [No Abstract]   [Full Text] [Related]  

  • 32. Demystifying standards: the six-step life cycle.
    Larrick K
    Biomed Instrum Technol; 2005; 39(6):483-4. PubMed ID: 17432474
    [No Abstract]   [Full Text] [Related]  

  • 33. FDA's revitalization of medical device review and regulation.
    Kessler DA
    Biomed Instrum Technol; 1994; 28(3):220-6. PubMed ID: 8061717
    [No Abstract]   [Full Text] [Related]  

  • 34. Using 80001 to manage medical devices on the IT network.
    Grimes SL
    Biomed Instrum Technol; 2011; Suppl():23-6. PubMed ID: 21992041
    [No Abstract]   [Full Text] [Related]  

  • 35. The essential element of ethics.
    Donawa ME
    Med Device Technol; 2004 Jun; 15(5):27-9. PubMed ID: 15285485
    [TBL] [Abstract][Full Text] [Related]  

  • 36. FDA lays out rules for regulating mobile medical apps.
    Mitka M
    JAMA; 2013 Nov; 310(17):1783-4. PubMed ID: 24193064
    [No Abstract]   [Full Text] [Related]  

  • 37. Ask George.
    Mills G
    Biomed Instrum Technol; 2011; 45(2):87. PubMed ID: 21466315
    [No Abstract]   [Full Text] [Related]  

  • 38. Positive control material introduced to ASTM Hemolysis Standard.
    Stand News; 2000 Jan; 28(1):9-10. PubMed ID: 11829027
    [No Abstract]   [Full Text] [Related]  

  • 39. 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]  

  • 40. FDA has a change of heart.
    Neil R
    Mater Manag Health Care; 2006 May; 15(5):9. PubMed ID: 16761870
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.