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European Medicines Agency safety guidelines

European Medicines Agency—Committee for Proprietary Medicinal Products. Guideline on the Evaluation of Control Samples In Nonclincial Safety Studies Checking for Contamination with the Test Substance. CPMP/SWP/1094/04. 17 March 2005. http //www.emea.europa.eu/pdfs/human/swp/109404en.pdf... [Pg.90]

European Medicines Agency. 2011. ICH guideline S6 (Rl)—PrecUnical safety evaluation of biotechnology—Derived pharmaceuticals. Available from http // www.ema.europa.eu/docs/en GB/document library/Scientific guide-line/2009/09/WC500002828.pdf. Accessed Jime 2011. [Pg.336]

See other pages where European Medicines Agency safety guidelines is mentioned: [Pg.4]    [Pg.232]    [Pg.70]    [Pg.506]    [Pg.579]    [Pg.105]    [Pg.503]    [Pg.12]    [Pg.129]    [Pg.172]    [Pg.645]    [Pg.48]    [Pg.27]    [Pg.1670]    [Pg.98]    [Pg.204]    [Pg.262]    [Pg.209]    [Pg.88]    [Pg.15]    [Pg.18]    [Pg.61]    [Pg.62]    [Pg.65]    [Pg.2339]    [Pg.333]    [Pg.379]    [Pg.5]    [Pg.439]    [Pg.4]    [Pg.71]   
See also in sourсe #XX -- [ Pg.82 ]



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