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PUBMED FOR HANDHELDS

Journal Abstract Search


1231 related items for PubMed ID: 19691172

  • 21. Establishment of vaccination clinics; user fees for investigational new drug (IND) influenza vaccine services and vaccines. Interim final rule and request for comments.
    Centers for Disease Control and Prevention (CDC), Department of Health and Human Services (HHS).
    Fed Regist; 2005 Jan 25; 70(15):3490-3. PubMed ID: 15669145
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  • 23. Human subject protection; foreign clinical studies not conducted under an investigational new drug application. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2008 Apr 28; 73(82):22800-16. PubMed ID: 18567164
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  • 28. Requirements for submission of labeling for human prescription drugs and biologics in electronic format. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2003 Dec 11; 68(238):69009-20. PubMed ID: 14672084
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  • 30. Investigational new drug applications and new drug applications--FDA. Final rule.
    Fed Regist; 1998 Feb 11; 63(28):6854-62. PubMed ID: 10177736
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  • 32. 2004 update--180-day exclusivity under the Hatch-Waxman amendments to the federal Food, Drug, and Cosmetic Act.
    Lietzan EK.
    Food Drug Law J; 2004 Feb 11; 59(4):459-63. PubMed ID: 15875350
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  • 34. New drugs for human use; clarification of requirements for patent holder notification--FDA. Proposed rule.
    Fed Regist; 1998 Mar 06; 63(44):11174-7. PubMed ID: 10177511
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  • 35. Applications for Food and Drug Administration approval to market a new drug; postmarketing reports; reporting information about authorized generic drugs. Direct final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2008 Sep 29; 73(189):56487-91. PubMed ID: 18985960
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  • 37. They are from the government and they really are here to help you.
    Woosley RL.
    J Clin Pharmacol; 2008 Feb 29; 48(2):142-3. PubMed ID: 18199889
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