BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

145 related articles for article (PubMed ID: 34818475)

  • 1. A Divisive Ruling on Devices -
    Zettler PJ; Adashi EY; Cohen IG
    N Engl J Med; 2021 Dec; 385(26):2409-2411. PubMed ID: 34818475
    [No Abstract]   [Full Text] [Related]  

  • 2. The FDA, preemption, and the Supreme Court.
    Glantz LH; Annas GJ
    N Engl J Med; 2008 May; 358(18):1883-5. PubMed ID: 18450601
    [No Abstract]   [Full Text] [Related]  

  • 3. The 21st Century Cures Act.
    Calderwood SB; Murray BE; Chambers HF
    N Engl J Med; 2015 Oct; 373(17):1679. PubMed ID: 26488713
    [No Abstract]   [Full Text] [Related]  

  • 4. The 21st Century Cures Act.
    Kakkis E; Bronstein MG
    N Engl J Med; 2015 Oct; 373(17):1678. PubMed ID: 26488712
    [No Abstract]   [Full Text] [Related]  

  • 5. The 21st Century Cures Act.
    McClellan MB; Sigal EV
    N Engl J Med; 2015 Oct; 373(17):1677-8. PubMed ID: 26488711
    [No Abstract]   [Full Text] [Related]  

  • 6. The 21st Century Cures Act.
    Kesselheim AS; Avorn J
    N Engl J Med; 2015 Oct; 373(17):1679-80. PubMed ID: 26488710
    [No Abstract]   [Full Text] [Related]  

  • 7. User fees and beyond--the FDA Safety and Innovation Act of 2012.
    Kramer DB; Kesselheim AS
    N Engl J Med; 2012 Oct; 367(14):1277-9. PubMed ID: 23034017
    [No Abstract]   [Full Text] [Related]  

  • 8. The 21st Century Cures Act: can the regulatory framework survive the "cures"?
    Osorio-de-Castro CG; Caetano R; Pepe VL
    Cad Saude Publica; 2015 Sep; 31(9):1807-10. PubMed ID: 26578005
    [No Abstract]   [Full Text] [Related]  

  • 9. Pharmaceuticals and medical devices: FDA oversight. End-of-year issue brief.
    Chaps NA
    Issue Brief Health Policy Track Serv; 2010 Jan; ():1-31. PubMed ID: 20217914
    [No Abstract]   [Full Text] [Related]  

  • 10. The 21st Century Cures Act--Will It Take Us Back in Time?
    Avorn J; Kesselheim AS
    N Engl J Med; 2015 Jun; 372(26):2473-5. PubMed ID: 26039522
    [No Abstract]   [Full Text] [Related]  

  • 11. Ethics and the FDA.
    Fielder J
    IEEE Eng Med Biol Mag; 2006; 25(4):13-7. PubMed ID: 16898653
    [No Abstract]   [Full Text] [Related]  

  • 12. Ejecting the FDA from the courtroom.
    Lancet; 2004 Aug 21-27; 364(9435):638. PubMed ID: 15325808
    [No Abstract]   [Full Text] [Related]  

  • 13. FDA reform plan edges closer to realisation.
    Marx V
    Lancet; 2012 Jun; 379(9832):2135. PubMed ID: 22690392
    [No Abstract]   [Full Text] [Related]  

  • 14. Clarification: 510k is premarket notification; it provides no patent or FDA approval.
    Burkhart CG
    J Drugs Dermatol; 2008 Feb; 7(2):105. PubMed ID: 18335644
    [No Abstract]   [Full Text] [Related]  

  • 15. Relocating abroad. FDA sends staff overseas to help monitor imports.
    Lee J
    Mod Healthc; 2011 Oct; 41(43):32. PubMed ID: 22111150
    [No Abstract]   [Full Text] [Related]  

  • 16. FDA set to tighten guidelines on industry dissemination of information on unapproved uses of medical products.
    Lang L
    Gastroenterology; 2008 Apr; 134(4):905. PubMed ID: 18395067
    [No Abstract]   [Full Text] [Related]  

  • 17. Combination products regulation at the FDA.
    Lauritsen KJ; Nguyen T
    Clin Pharmacol Ther; 2009 May; 85(5):468-70. PubMed ID: 19381151
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Regulation of drugs and devices: an evolution.
    Merrill RA
    Health Aff (Millwood); 1994; 13(3):47-69. PubMed ID: 7927161
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Product safety and business interests: deja vu..
    Rijswijk L
    Ostomy Wound Manage; 2005 Feb; 51(2):8-9. PubMed ID: 15699549
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.