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PUBMED FOR HANDHELDS

Journal Abstract Search


267 related items for PubMed ID: 8361258

  • 1. 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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  • 4. Inspection of clinical investigations by the German health authorities.
    Schmidt M.
    Methods Find Exp Clin Pharmacol; 1993 May; 15(4):229-31. PubMed ID: 8361260
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  • 5. [Community requirements relating to drugs derived from human blood and plasma].
    Brunko P.
    Ann Pharm Fr; 1994 May; 52(2):89-98. PubMed ID: 7944184
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  • 7. Establishing pan-European clinical trials: regulatory compliance and other practical considerations.
    Grienenberger A.
    J Biolaw Bus; 2004 May; 7(4):58-63. PubMed ID: 15675097
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  • 12. [Harmonisation of regulatory requirements for clinical trials on medicinal products for human use in the Directive 2001/20/EC and complementary guidance. Implementation of the 12th Law Amending the German Drug Law].
    Geisler I, Hofmann HP, Nickel L.
    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2005 Feb; 48(2):141-6. PubMed ID: 15726454
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  • 15. [ICH-GCP Guideline: quality assurance of clinical trials. Status and perspectives].
    Englev E, Petersen KP.
    Ugeskr Laeger; 2003 Apr 14; 165(16):1659-62. PubMed ID: 12756823
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  • 18. [The role of ethical committees in drug trials performed according to "Good Clinical Practice"].
    Kerpel-Fronius S.
    Orv Hetil; 1991 Mar 31; 132(13):703-5. PubMed ID: 2014128
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  • 20. [Good clinical practice. Requirements for clinical documentation on the introduction of new drugs].
    Dirach J.
    Ugeskr Laeger; 1990 Apr 02; 152(14):992-4. PubMed ID: 2183456
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