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Journal Abstract Search

132 related items for PubMed ID: 20347331

  • 1. Low levels of extraneous agents in vaccine starting materials.
    Rouby JC.
    Biologicals; 2010 May; 38(3):354-7. PubMed ID: 20347331
    [Abstract] [Full Text] [Related]

  • 2. Tracing and control of raw materials sourcing for vaccine manufacturers.
    Faretra Peysson L.
    Biologicals; 2010 May; 38(3):352-3. PubMed ID: 20335052
    [Abstract] [Full Text] [Related]

  • 3. Extraneous agents testing for substrates of avian origin and viral vaccines for poultry: current provisions and proposals for future approaches.
    Jungbäck C, Motitschke A.
    Biologicals; 2010 May; 38(3):362-5. PubMed ID: 20335053
    [Abstract] [Full Text] [Related]

  • 4. Risk reduction in biotherapeutic products.
    Ill CR, Dehghani H.
    Curr Opin Drug Discov Devel; 2009 Mar; 12(2):296-304. PubMed ID: 19333875
    [Abstract] [Full Text] [Related]

  • 5. Viral safety and extraneous agents testing for veterinary vaccines: rationale for requirements, the European approach.
    Bruckner L.
    Biologicals; 2010 May; 38(3):338-9. PubMed ID: 20335051
    [Abstract] [Full Text] [Related]

  • 6. Current challenges in viral safety and extraneous agent testing.
    Mackay D, Kriz N.
    Biologicals; 2010 May; 38(3):335-7. PubMed ID: 20338787
    [Abstract] [Full Text] [Related]

  • 7. Comparison of requirements in the European Union and United States of America for pre-clinical viral safety testing of veterinary vaccines.
    Sheridan S, Coughlin J.
    Biologicals; 2010 May; 38(3):340-5. PubMed ID: 20400329
    [Abstract] [Full Text] [Related]

  • 8. Three Rs potential in the development and quality control of immunobiologicals.
    Halder M.
    ALTEX; 2001 May; 18 Suppl 1():13-47. PubMed ID: 11854853
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  • 12. Organic solvents in the pharmaceutical industry.
    Grodowska K, Parczewski A.
    Acta Pol Pharm; 2010 May; 67(1):3-12. PubMed ID: 20210074
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  • 13. Transmissible spongiform encephalopathies (TSE): minimizing the risk of transmission by biological/biopharmaceutical products: an industry perspective.
    Kozak RW, Golker CF, Stadler P.
    Dev Biol Stand; 1996 May; 88():257-64. PubMed ID: 9119148
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  • 16. Anticancer Drug Development: The Way Forward.
    Connors T.
    Oncologist; 1996 May; 1(3):180-181. PubMed ID: 10387985
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  • 17. Ensuring the quality, potency and safety of vaccines during preclinical development.
    Lebron JA, Wolf JJ, Kaplanski CV, Ledwith BJ.
    Expert Rev Vaccines; 2005 Dec; 4(6):855-66. PubMed ID: 16372881
    [Abstract] [Full Text] [Related]

  • 18. Adventitious agents from animal-derived raw materials--a method of risk assessment.
    Foster LG.
    Dev Biol Stand; 1996 Dec; 88():283-90. PubMed ID: 9119152
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  • 19. Who Expert Committee on Biological Standardization.
    World Health Organization.
    World Health Organ Tech Rep Ser; 2004 Dec; 926():1-109. PubMed ID: 15918537
    [Abstract] [Full Text] [Related]

  • 20. Technical Report No. 38. Manufacturing chromatography systems postapproval changes (ChromPAC): chemistry, manufacturing, and controls documentation.
    PDA Manufacturing Chromatography Systems PAC Taskforce.
    PDA J Pharm Sci Technol; 2006 Mar; 60(1 Suppl TR38):1-29. PubMed ID: 16696189
    [No Abstract] [Full Text] [Related]

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