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 *

212 related articles for article (PubMed ID: 10126251)

  • 1. The 21 CFR (Code of Federal Regulations) online database: Food and Drug Administration regulations full-text.
    Bobka MS
    Med Ref Serv Q; 1993; 12(1):7-15. PubMed ID: 10126251
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Export of pharmaceuticals and medical devices under the federal Food, Drug & Cosmetic Act: FDA's striking change in interpretation post-Shelhigh.
    Basile EM; Tolomeo D; Gluck E
    Food Drug Law J; 2009; 64(1):149-69. PubMed ID: 19998744
    [TBL] [Abstract][Full Text] [Related]  

  • 3. US regulation of combination products.
    Donawa M
    Med Device Technol; 2009 Oct; 20(6):22, 24-5. PubMed ID: 20302139
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Demystifying 21 CFR Part 556--tolerances for residues of new animal drugs in food.
    Brynes SD
    Regul Toxicol Pharmacol; 2005 Aug; 42(3):324-7. PubMed ID: 16006026
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Supplemental applications proposing labeling changes for approved drugs, biologics, and medical devices. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2008 Aug; 73(164):49603-10. PubMed ID: 18958946
    [TBL] [Abstract][Full Text] [Related]  

  • 6. FDA's proposed regulations to expand access to investigational drugs for treatment use: the status quo in the guise of reform.
    Rossen BR
    Food Drug Law J; 2009; 64(1):183-223. PubMed ID: 19998746
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Delegations of authority and organization; Office of the Commissioner--FDA. Final rule.
    Fed Regist; 1991 Nov; 56(225):58758. PubMed ID: 10115698
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Drugs and other product choices.
    Hyman PM; Carvajal R
    Dermatol Ther; 2009; 22(3):216-24. PubMed ID: 19453345
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Food and Drug Administration--part I: Federal agency close-up.
    Kauffman NM; Malevich S; Smith DJ; Petersen-Kauffman LC
    Am J Med Technol; 1980 Jun; 46(6):428-36. PubMed ID: 7386516
    [No Abstract]   [Full Text] [Related]  

  • 11. Pharmaceuticals and medical devices: medical devices.
    Chaps NA
    Issue Brief Health Policy Track Serv; 2009 Jan; ():1-23. PubMed ID: 19297720
    [No Abstract]   [Full Text] [Related]  

  • 12. Medical devices and the US Food and Drug Administration: regulating the tools of radiology.
    Henderson JA; Smith JJ
    J Am Coll Radiol; 2005 Jun; 2(6):504-10. PubMed ID: 17411867
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The financing and regulation of medical devices in the United States.
    Sisk JE
    Med Prog Technol; 1982; 9(2-3):181-6. PubMed ID: 7162490
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The Food and Drug Administration and the backward motion toward the source.
    Kennedy D
    Public Health Rep; 1978; 93(6):607-15. PubMed ID: 362468
    [No Abstract]   [Full Text] [Related]  

  • 15. Pharmaceuticals and medical devices: medical devices. Year end issue brief.
    Tiffany S
    Issue Brief Health Policy Track Serv; 2008 Jan; ():1-19. PubMed ID: 18345548
    [No Abstract]   [Full Text] [Related]  

  • 16. Medical devices; preemption of state product liability claims--FDA. Proposed rule.
    Fed Regist; 1997 Dec; 62(239):65384-8. PubMed ID: 10176832
    [TBL] [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. Economic cost for implementation of the U.S. Food and Drug Administration's Code of Federal Regulations Title 21, Part 1271 in an egg donor program.
    Baker VL; Gvakharia MO; Rone HM; Manalad JR; Adamson GD
    Fertil Steril; 2008 Sep; 90(3):537-45. PubMed ID: 17953961
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Medical devices; reclassification and codification of the stainless steel suture. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Apr; 65(72):19835-6. PubMed ID: 11010635
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.