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PUBMED FOR HANDHELDS

Journal Abstract Search


274 related items for PubMed ID: 17252718

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  • 3. Non-clinical Post-Marketing Commitments for newly licenced pharmaceuticals.
    Reeve LM.
    Regul Toxicol Pharmacol; 2009 Nov; 55(2):181-7. PubMed ID: 19589365
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  • 4. Procedures and methods of benefit assessments for medicines in Germany.
    Bekkering GE, Kleijnen J.
    Eur J Health Econ; 2008 Nov; 9 Suppl 1():5-29. PubMed ID: 18987905
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  • 6. Granting marketing authorisation for medicines in South East European countries: the point of view of the authority.
    Tomić S, Sucić AF, Martinac AI.
    Regul Toxicol Pharmacol; 2010 Nov; 57(2-3):325-32. PubMed ID: 20385190
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  • 9. Regulatory pathways for vaccines for developing countries.
    Milstien J, Belgharbi L.
    Bull World Health Organ; 2004 Feb; 82(2):128-33. PubMed ID: 15042235
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  • 10. [Procedures and methods of benefit assessments for medicines in Germany].
    Bekkering GE, Kleijnen J.
    Dtsch Med Wochenschr; 2008 Dec; 133 Suppl 7():S225-46. PubMed ID: 19034813
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  • 12. Lessons learned from independent central review.
    Ford R, Schwartz L, Dancey J, Dodd LE, Eisenhauer EA, Gwyther S, Rubinstein L, Sargent D, Shankar L, Therasse P, Verweij J.
    Eur J Cancer; 2009 Jan; 45(2):268-74. PubMed ID: 19101138
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  • 16. European regulatory guidelines for biosimilars.
    Wiecek A, Mikhail A.
    Nephrol Dial Transplant; 2006 Oct; 21 Suppl 5():v17-20. PubMed ID: 16959790
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  • 18. [Approval of drugs by national and European agencies--sequelae for the pharmaceutical industry].
    Zierenberg O.
    Z Arztl Fortbild Qualitatssich; 1997 Nov; 91(7):596-600. PubMed ID: 9527448
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