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Journal Abstract Search

174 related items for PubMed ID: 9527447

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  • 4. [New drugs and European procedures of approval. The European Agency for the Evaluation of Medicinal Products' role].
    Ainsworth MA.
    Ugeskr Laeger; 2003 Apr 14; 165(16):1648-9. PubMed ID: 12756819
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  • 6. The regulatory system in europe with special emphasis on allergen products.
    Lorenz AR, Luttkopf D, Seitz R, Vieths S.
    Int Arch Allergy Immunol; 2008 Apr 14; 147(4):263-75. PubMed ID: 18648190
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  • 7. [European drug policy].
    Sauer F.
    Bull Mem Acad R Med Belg; 1993 Apr 14; 148(5-6):207-12; discussion 212-6. PubMed ID: 8142930
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  • 8. [Registration of new medicinal products in Europe].
    Singer E.
    Onkologie; 2008 Apr 14; 31 Suppl 2():64-6. PubMed ID: 18487872
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  • 9. [Scientific advice by the nationally competent authority and by the EMEA on the conduct of clinical trials].
    Dejas-Eckertz P, Schäffner G.
    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2005 Apr 14; 48(4):423-8. PubMed ID: 15830253
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  • 10. [Drugs in Europe].
    Bouzy C, Abadie E.
    Rev Prat; 2002 Mar 01; 52(5):510-4. PubMed ID: 11949504
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  • 11. Medicines for children licensed by the European Agency for the Evaluation of Medicinal Products.
    Ceci A, Felisi M, Catapano M, Baiardi P, Cipollina L, Ravera S, Bagnulo S, Reggio S, Rondini G.
    Eur J Clin Pharmacol; 2002 Nov 01; 58(8):495-500. PubMed ID: 12451425
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  • 12. [Safety monitoring of cell-based medicinal products (CBMPs)].
    Funk MB, Frech M, Spranger R, Keller-Stanislawski B.
    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2015 Nov 01; 58(11-12):1239-46. PubMed ID: 26391098
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  • 13. [Approval of drugs by national and European agencies--from the viewpoint of drug approval committee A].
    Henschler D.
    Z Arztl Fortbild Qualitatssich; 1997 Nov 01; 91(7):600-3. PubMed ID: 9527449
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  • 14. [Review of the development in European Legislation on the harmonisation of the laws for medicinal products].
    Lehmann B.
    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2008 Jul 01; 51(7):713-21. PubMed ID: 18584107
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  • 15. Marketing authorization of veterinary medicinal products in Poland.
    Sztabińska-Koncka H, Lewicki J.
    Regul Toxicol Pharmacol; 1997 Aug 01; 26(1 Pt 1):129-33. PubMed ID: 9339489
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  • 16. Legal requirements for the quality of herbal substances and herbal preparations for the manufacturing of herbal medicinal products in the European union.
    Vlietinck A, Pieters L, Apers S.
    Planta Med; 2009 Jun 01; 75(7):683-8. PubMed ID: 19204891
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  • 17. Non-clinical Post-Marketing Commitments for newly licenced pharmaceuticals.
    Reeve LM.
    Regul Toxicol Pharmacol; 2009 Nov 01; 55(2):181-7. PubMed ID: 19589365
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  • 20. EMEA (European Medicines Evaluation Agency) and the new pharmaceutical procedures for Europe.
    Jones K, Jefferys D.
    Health Trends; 1994 Nov 01; 26(1):10-3. PubMed ID: 10171959
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