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 *

141 related articles for article (PubMed ID: 1594477)

  • 1. Using the FDA's Device Experience Network.
    Collins JL
    Oncol Nurs Forum; 1992 Apr; 19(3):524. PubMed ID: 1594477
    [No Abstract]   [Full Text] [Related]  

  • 2. FDA's medical device standards policy.
    Stimson RA
    J Parenter Sci Technol; 1981; 35(2):60-2. PubMed ID: 7229834
    [No Abstract]   [Full Text] [Related]  

  • 3. Is FDA's medical device evaluation process overly complaisant to industry?
    Margolis RE
    Healthspan; 1992; 9(7):19-20. PubMed ID: 10121440
    [No Abstract]   [Full Text] [Related]  

  • 4. FDA's developing standards policy.
    Link DM
    Med Instrum; 1979; 13(4):196-7. PubMed ID: 470656
    [No Abstract]   [Full Text] [Related]  

  • 5. FDA's focus on consensus standards: the vision, the heartbreak, the hope.
    Altman MR; Marlowe DE
    Stand News; 1999 May; 27(5):24-5. PubMed ID: 10558422
    [No Abstract]   [Full Text] [Related]  

  • 6. FDA's Quality System Inspection Technique in Ireland.
    Higgins S
    Med Device Technol; 2001; 12(1):40-1. PubMed ID: 11317865
    [No Abstract]   [Full Text] [Related]  

  • 7. Voluntary consensus standards and the FDA's regulatory program.
    Gardner S
    Med Instrum; 1979; 13(4):239-42. PubMed ID: 470665
    [No Abstract]   [Full Text] [Related]  

  • 8. FDA's performance standard for electrode lead wires and patient cables. Second phase is now being implemented.
    Health Devices; 2000 Apr; 29(4):140-1. PubMed ID: 11002440
    [No Abstract]   [Full Text] [Related]  

  • 9. ECRI to clinical engineering departments: "heads up! ... FDA's potential regulation of servicers, remarketers, and refurbishers could affect you".
    Health Devices; 1998 Aug; 27(8):276. PubMed ID: 9743899
    [No Abstract]   [Full Text] [Related]  

  • 10. Medical devices; medical device reporting. Direct final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2005 Feb; 70(38):9516-28. PubMed ID: 15736310
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Computerized medical device tracking--ways to comply with SMDA (Safe Medical Devices Act of 1990).
    Landis D
    Healthc Inform; 1992 Jul; 9(7):36, 38, 40-2. PubMed ID: 10119858
    [No Abstract]   [Full Text] [Related]  

  • 12. Jay Crowley the FDA's perspective on the unique device identification system.
    Crowley J
    Healthc Financ Manage; 2009 Sep; 63(9):48-51. PubMed ID: 19743648
    [No Abstract]   [Full Text] [Related]  

  • 13. Guidance for the emergency use of unapproved medical devices; availability--FDA. Notice.
    Fed Regist; 1985 Oct; 50(204):42866-7. PubMed ID: 10274027
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The Safe Medical Devices Act of 1990--FDA. Notice.
    Fed Regist; 1991 Apr; 56(66):14111-3. PubMed ID: 10111151
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Upon closer inspection. As the U.S. imports more drugs and devices, the FDA's overseas initiatives aim to head off trouble at the source.
    Rhea S
    Mod Healthc; 2009 Mar; 39(13):28-30. PubMed ID: 19405431
    [No Abstract]   [Full Text] [Related]  

  • 16. Amendment of various device regulations to reflect current American Society for Testing and Material citations. Food and Drug Administration, HHS. Direct final rule.
    Fed Regist; 2000 Jan; 65(15):3584-5. PubMed ID: 11010654
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. FDA's proposed regulatory approach to regulation of hematopoietic stem/progenitor cell products.
    Harvath L
    Cytotherapy; 1999; 1(4):358-9. PubMed ID: 20440912
    [No Abstract]   [Full Text] [Related]  

  • 19. Delegations of authority and organization; Center for Devices and Radiological Health--FDA. Final rule.
    Fed Regist; 1991 Oct; 56(197):51169-70. PubMed ID: 10115059
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Medical device vigilance at FDA.
    Gross TP; Kessler LG
    Stud Health Technol Inform; 1996; 28():17-24. PubMed ID: 10164091
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.