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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

2165 related items for PubMed ID: 19998744

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  • 3. 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
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  • 4. Import for export; reporting and recordkeeping requirements for unapproved or violative products imported for further processing or incorporation and subsequent export--FDA. Proposed rule.
    Fed Regist; 1998 Nov 24; 63(226):64930-7. PubMed ID: 10338872
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  • 6. Draft guidance for industry; exports and imports under the FDA Export Reform and Enhancement Act of 1996--FDA. Notice.
    Fed Regist; 1998 Jun 12; 63(113):32219-34. PubMed ID: 10180275
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  • 7. Medical devices; humanitarian use of devices--FDA. Direct final rule.
    Fed Regist; 1998 Apr 17; 63(74):19185-90. PubMed ID: 10178430
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  • 8. Medical device labeling and advertising: an overview.
    Basile EM, Armentrout E, Reeves KN.
    Food Drug Law J; 1999 Apr 17; 54(4):519-33. PubMed ID: 11824451
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  • 10. Gastroenterology-urology devices; effective date of requirement for premarket approval of the penile inflatable implant. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Apr 12; 65(71):19650-8. PubMed ID: 11010632
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  • 12. Medical device reporting: manufacturer reporting, importer reporting, user facility reporting, and distributor reporting--FDA. Direct final rule.
    Fed Regist; 1998 May 12; 63(91):26069-77. PubMed ID: 10179334
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  • 14. Medical devices; 30-day notices and 135-day PMA (premarket approval application) supplement review--FDA. Direct final rule.
    Fed Regist; 1998 Apr 27; 63(80 Pt 1):20530-3. PubMed ID: 10179319
    [Abstract] [Full Text] [Related]

  • 15. Investigational new drugs: export requirements for unapproved new drug products. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2005 Nov 23; 70(225):70720-30. PubMed ID: 16304736
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  • 16. Guidance of FDA's expectations of medical device manufacturers concerning the year 2000 date problem--FDA. Notice.
    Fed Regist; 1998 Jun 24; 63(121):34433-42. PubMed ID: 10180297
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  • 17. Medical devices; medical device reporting; baseline reports. Direct final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2008 Jun 13; 73(115):33692-5. PubMed ID: 18677824
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  • 18. Medical devices; device tracking; new orders to manufacturers--FDA. Notice.
    Fed Regist; 1998 Mar 04; 63(42):10638-40. PubMed ID: 10177504
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  • 19. FDA's expanding postmarket authority to monitor and publicize food and consumer health product risks: the need for procedural safeguards to reduce "transparency" policy harms in the post-9/11 regulatory environment.
    Roller ST, Pippins RR, Ngai JW.
    Food Drug Law J; 2009 Mar 04; 64(3):577-98. PubMed ID: 19999646
    [Abstract] [Full Text] [Related]

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