BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

140 related articles for article (PubMed ID: 10147069)

  • 1. Sterilizers and the medical device directive.
    Donawa ME
    Med Device Technol; 1994 May; 5(4):10, 12. PubMed ID: 10147069
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Baby doe redux? The Department of Health and Human Services and the Born-Alive Infants Protection Act of 2002: a cautionary note on normative neonatal practice.
    Sayeed SA
    Pediatrics; 2005 Oct; 116(4):e576-85. PubMed ID: 16199687
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Warning! AbTox sterilizers recalled--FDA is on the case.
    Blyth PL
    Mater Manag Health Care; 1998 Jun; 7(6):16. PubMed ID: 10183406
    [No Abstract]   [Full Text] [Related]  

  • 4. Medical devices; medical device reporting; baseline reports. Direct final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2008 Jun; 73(115):33692-5. PubMed ID: 18677824
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The impact of regulation.
    Magazine AH
    Med Device Technol; 1997 Mar; 8(2):38-44, 46, 48. PubMed ID: 10166366
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Implementation of the mutual recognition agreement between the United States and the European Community; pharmaceutical GMP's and medical devices; establishment of a public docket and FDA contact points. Food and Drug Administration, HHS. Establishment of a public docket and FDA contact points.
    Fed Regist; 1999 Mar; 64(45):11376-7. PubMed ID: 10557625
    [TBL] [Abstract][Full Text] [Related]  

  • 7. FDA modernization act of 1997: guidance on medical device tracking; availability--FDA. Notice.
    Fed Regist; 1998 Mar; 63(42):10640-1. PubMed ID: 10177505
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Refurbished medical equipment.
    Donawa ME
    Med Device Technol; 1998 Apr; 9(3):12-5. PubMed ID: 10179194
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Making sense of the food and drug administration.
    Connor JA
    Semin Pediatr Surg; 2006 Nov; 15(4):293-301. PubMed ID: 17055960
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Medical devices: the obvious, the readily-accepted, and the surprising.
    Tolomeo DE; Clarke LA
    J Health Life Sci Law; 2008 Jul; 1(4):117, 119-44. PubMed ID: 18717154
    [TBL] [Abstract][Full Text] [Related]  

  • 11. US FDA perspective on the regulations of medical-grade polymers: cyanoacrylate polymer medical device tissue adhesives.
    Mattamal GJ
    Expert Rev Med Devices; 2008 Jan; 5(1):41-9. PubMed ID: 18095895
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Standards for humidification and filtration devices.
    Stevens J
    Respir Care Clin N Am; 2006 Jun; 12(2):203-32. PubMed ID: 16828691
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutual Recognition of the Food and Drug Administration and European Community Member State Conformity Assessment Procedures; pharmaceutical GMP inspection reports, medical device quality system evaluation reports, and certain medical device premarket evaluation reports--FDA. Proposed rule.
    Fed Regist; 1998 Apr; 63(69):17744-71. PubMed ID: 10177764
    [TBL] [Abstract][Full Text] [Related]  

  • 14. View from the Nation's Capital. FDA challenged successfully on its policies regarding good manufacturing practice inspections of medical drug and device manufacturers.
    Appler WD
    J Clin Psychopharmacol; 1987 Oct; 7(5):346-7. PubMed ID: 3680606
    [No Abstract]   [Full Text] [Related]  

  • 15. Medical device reporting--FDA. Reproposal.
    Fed Regist; 1983 May; 48(104):24014-24. PubMed ID: 10261480
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [The origin of informed consent].
    Mallardi V
    Acta Otorhinolaryngol Ital; 2005 Oct; 25(5):312-27. PubMed ID: 16602332
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutual recognition of pharmaceutical good manufacturing practice inspection reports, medical device quality system audit reports, and certain medical device product evaluation reports between the United States and the European Community--FDA. Final rule.
    Fed Regist; 1998 Nov; 63(215):60122-64. PubMed ID: 10187390
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The history and contemporary challenges of the US Food and Drug Administration.
    Borchers AT; Hagie F; Keen CL; Gershwin ME
    Clin Ther; 2007 Jan; 29(1):1-16. PubMed ID: 17379043
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Medical devices: cardiovascular devices: reclassification of the arrhythmia detector and alarm. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2003 Oct; 68(208):61342-4. PubMed ID: 14584507
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Regulatory initiatives for natural latex allergy: US perspectives.
    Farnham JJ; Tomazic-Jezic VJ; Stratmeyer ME
    Methods; 2002 May; 27(1):87-92. PubMed ID: 12079422
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.