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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

399 related items for PubMed ID: 12356093

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  • 2. International Cooperation on Harmonisation of Technical requirements for Approval of Veterinary Medicinal Products (VICH); final guidance on " Safety studies for veterinary drug residues in human food: reproduction toxicity testing" (VICH GL22); availability. Notice.
    Food and Drug Administration, HHS.
    Fed Regist; 2002 Jan 04; 67(3):603-5. PubMed ID: 12365425
    [Abstract] [Full Text] [Related]

  • 3. International Conference on Harmonisation: guidance on testing for carcinogenicity of pharmaceuticals. Notice. Food and Drug Administration, HHS.
    Fed Regist; 1998 Feb 23; 63(35):8983-6. PubMed ID: 12269370
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  • 6. International Conference on Harmonisation; guidance on specifications: test procedures and acceptance criteria for biotechnological/biological products. Notice. Food and Drug Administration, HHS.
    Fed Regist; 1999 Aug 18; 64(159):44928-35. PubMed ID: 12356094
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  • 7. International Conference on Harmonisation; Guidance on S8 Immunotoxicity Studies for Human Pharmaceuticals; availability. Notice.
    Food and Drug Administration, HHS.
    Fed Regist; 2006 Apr 13; 71(71):19193-4. PubMed ID: 16612859
    [Abstract] [Full Text] [Related]

  • 8. International Conference on Harmonisation; evaluation of stability data; availability. Notice.
    Food and Drug Administration, HHS.
    Fed Regist; 2004 Jun 08; 69(110):32010-1. PubMed ID: 15185712
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  • 10. International Cooperation on Harmonisation of Technical Requirements for Approval of Veterinary Medicinal Products (VICH); final guidance for industry on "studies to evaluate the safety of residues of veterinary drugs in human food: genotoxicity testing" (VICH GL23); availability. Notice.
    Food and Drug Administration, HHS.
    Fed Regist; 2002 Jan 04; 67(3):602-3. PubMed ID: 12358039
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  • 13. International Conference on Harmonisation; guidance on Q6A specifications: test procedures and acceptance criteria for new drug substances and new drug products: chemical substances. Notice.
    Food and Drug Administration, HHS.
    Fed Regist; 2000 Dec 29; 65(251):83041-63. PubMed ID: 12356095
    [Abstract] [Full Text] [Related]

  • 14. International Conference on Harmonisation; choice of control group and related issues in clinical trials; availability. Notice.
    Food and Drug Administration, HHS.
    Fed Regist; 2001 May 14; 66(93):24390-1. PubMed ID: 12356096
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  • 15. International Conference on Harmonisation; Guidance on S9 Nonclincal Evaluation for Anticancer Pharmaceuticals; availability. Notice.
    Food and Drug Administration, HHS.
    Fed Regist; 2010 Mar 08; 75(44):10487-8. PubMed ID: 20383918
    [Abstract] [Full Text] [Related]

  • 16. International Conference on Harmonisation; Guidance on Q4B Evaluation and Recommendation of Pharmacopoeial Texts for Use in the International Conference on Harmonisation Regions; Annex 7 on Dissolution Test General Chapter; availability. Notice.
    Food and Drug Administration, HHS.
    Fed Regist; 2010 Apr 05; 75(64):17148-9. PubMed ID: 20383923
    [Abstract] [Full Text] [Related]

  • 17. International Conference on Harmonisation; guidance on M4 common technical document; availability. Notice.
    Food and Drug Administration, HHS.
    Fed Regist; 2001 Oct 16; 66(200):52634-7. PubMed ID: 12358037
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  • 19. International Conference on Harmonisation; Guidance on Q4B Evaluation and Recommendation of Pharmacopoeial Texts for Use in the International Conference on Harmonisation Regions; availability. Notice.
    Food and Drug Administration, HHS.
    Fed Regist; 2008 Feb 21; 73(35):9575-6. PubMed ID: 18677819
    [Abstract] [Full Text] [Related]

  • 20. International Conference on Harmonisation; guidance on Addendum to E2C Clinical Safety Data Management: Periodic Safety Update Reports for Marketed Drugs; availability. Notice.
    Food and Drug Administration, HHS.
    Fed Regist; 2004 Feb 05; 69(24):5551-2. PubMed ID: 14968802
    [Abstract] [Full Text] [Related]

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