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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

313 related items for PubMed ID: 17847577

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  • 4. Revisions to the requirements applicable to blood, blood components, and source plasma; confirmation in part and technical amendment. Food and Drug Administration, HHS. Direct final rule; confirmation in part and technical amendment.
    Fed Regist; 2001 Jan 10; 66(7):1834-7. PubMed ID: 11503754
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  • 7. Revisions to the requirements applicable to blood, blood components and source plasma; confirmation of effective date and technical amendment. Direct final rule; confirmation of effective date and technical amendment.
    Food and Drug Administration, HHS.
    Fed Regist; 2008 Feb 08; 73(27):7463-4. PubMed ID: 18389917
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  • 8. Revisions to the requirements applicable to blood, blood components, and source plasma. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2001 Aug 06; 66(151):40886-90. PubMed ID: 11732557
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  • 12. Revisions to the general safety requirements for biological products--FD. Direct final rule.
    Fed Regist; 1998 Apr 20; 63(75):19399-403. PubMed ID: 10178869
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  • 13. Blood vessels recovered with organs and intended for use in organ transplantation. Direct final rule.
    Food and Drug Administration, Health Resources and Services Administration, (HHS).
    Fed Regist; 2006 May 12; 71(92):27606-10. PubMed ID: 16696153
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  • 14. Amendment to examination and investigation sample requirements--FDA. Direct final rule.
    Fed Regist; 1998 Sep 25; 63(186):51297-9. PubMed ID: 10185810
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  • 15. Revision of requirements applicable to albumin (human), plasma protein fraction (human), and immune globulin (human); confirmation in part and technical amendment. Food and Drug Administration, HHS. Direct final rule; confirmation in part and technical amendment.
    Fed Regist; 2000 Mar 14; 65(50):13678-9. PubMed ID: 11010647
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  • 16. Revision of requirements applicable to albumin (human), plasma protein fraction (human), and immune globulin (human). Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Aug 28; 65(167):52016-8. PubMed ID: 11067735
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  • 17. Current good manufacturing practices for blood and blood components: notification of consignees receiving blood and blood components at increased risk for transmitting HIV infection--FDA. Final rule.
    Fed Regist; 1996 Sep 09; 61(175):47413-23. PubMed ID: 10160337
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  • 18. 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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  • 19. Medical devices; hearing aids; technical data amendments. Direct final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2008 Jun 02; 73(106):31358-60. PubMed ID: 18677822
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  • 20. Requirements for testing human blood donors for evidence of infection due to communicable disease agents. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2001 Jun 11; 66(112):31146-65. PubMed ID: 11725786
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