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PUBMED FOR HANDHELDS

Journal Abstract Search


408 related items for PubMed ID: 7944184

  • 1. [Community requirements relating to drugs derived from human blood and plasma].
    Brunko P.
    Ann Pharm Fr; 1994; 52(2):89-98. PubMed ID: 7944184
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  • 4. European project concerning the guidelines on medicinal products derived from human blood and plasma.
    Horaud F.
    Dev Biol Stand; 1991; 75():237-40. PubMed ID: 1794627
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  • 6. [Regulations on gases for medical use in France].
    Poitou P, Fouret C, Duffau E.
    Ann Pharm Fr; 2002 Sep; 60(5):326-32. PubMed ID: 12378142
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  • 7. The European Blood Directive--its role in blood safety.
    Seitz R.
    Dev Biol (Basel); 2007 Sep; 127():147-52. PubMed ID: 17486887
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  • 14. The development of good clinical practice in the EEC and in Germany.
    Anhalt E.
    Methods Find Exp Clin Pharmacol; 1993 May; 15(4):217-22. PubMed ID: 8361258
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  • 15. Current guidelines applicable for the approval of topically applied dermatological drugs in the EU.
    Straube MD, Zesch A.
    Fundam Clin Pharmacol; 2004 Oct; 18(5):503-11. PubMed ID: 15482371
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  • 16. Animal welfare and protection during transport: the current legislative framework in European Union.
    Passantino A.
    Ann Ist Super Sanita; 2006 Oct; 42(2):222-30. PubMed ID: 17033144
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  • 17. 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; 75(7):683-8. PubMed ID: 19204891
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  • 18. [The new norms decreed by the legislative dirrective 91-93 CCE].
    Neri M, Palazzo S.
    Boll Chim Farm; 1998 Feb; 137(2):31-4. PubMed ID: 9595832
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  • 19. [Status of law-making on animal welfare].
    Polten B.
    Dtsch Tierarztl Wochenschr; 2007 Mar; 114(3):98-103. PubMed ID: 17419542
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  • 20. Good manufacturing practice for immunological veterinary medicinal products.
    Todd JI.
    Rev Sci Tech; 2007 Apr; 26(1):135-45. PubMed ID: 17633298
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