{"id":7285,"date":"2023-06-14T14:20:59","date_gmt":"2023-06-14T12:20:59","guid":{"rendered":"https:\/\/www.sciencepharma.pl\/?post_type=pharmacovigilance&#038;p=7285"},"modified":"2023-12-12T13:44:26","modified_gmt":"2023-12-12T12:44:26","slug":"glp","status":"publish","type":"pharmacovigilance","link":"https:\/\/www.sciencepharma.com\/pl\/services\/glp\/","title":{"rendered":"GLP"},"content":{"rendered":"\n<h1 class=\"wp-block-heading\">GLP<\/h1>\n\n\n<p style=\"text-align: justify;\">W celu zapewnienia jako\u015bci bada\u0144 nieklinicznych oraz oznacze\u0144 bioanalitycznych w badaniach klinicznych wszystkie wymienione badania powinny by\u0107 prowadzone zgodnie z zasadami Dobrej Praktyki Laboratoryjnej (GLP).<\/p>\n<p style=\"text-align: justify;\">SciencePharma dysponuje do\u015bwiadczonym zespo\u0142em audytor\u00f3w posiadaj\u0105cych szerok\u0105 wiedz\u0119 w zakresie prowadzenia nieklinicznych bada\u0144 in vitro i in vivo oraz wykonywania analiz pr\u00f3bek pobranych od uczestnik\u00f3w bada\u0144 klinicznych zar\u00f3wno metodami chromatograficznymi, jak i biologicznymi.<\/p>\n<p style=\"text-align: justify;\">Oferujemy audyty system\u00f3w jako\u015bci na zgodno\u015b\u0107 z zaleceniami DPL, podczas kt\u00f3rych weryfikowane s\u0105 standardowe procedury dzia\u0142ania i dokumenty z nimi zwi\u0105zane, ale tak\u017ce sama organizacja, kwalifikacje personelu, spos\u00f3b prowadzenia bada\u0144 i prowadzenia dokumentacji. System audyt\u00f3w GLP jest bardzo przydatnym narz\u0119dziem w doborze podwykonawc\u00f3w.<\/p>\n\n\n<p><\/p>\n\n\n\n<p><a href=\"https:\/\/www.sciencepharma.com\/pl\/services\/audyty-glp-zdalnie-i-stacjonarnie\/\">Wi\u0119cej<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>GLP W celu zapewnienia jako\u015bci bada\u0144 nieklinicznych oraz oznacze\u0144 bioanalitycznych w badaniach klinicznych wszystkie wymienione badania powinny by\u0107 prowadzone zgodnie z zasadami Dobrej Praktyki Laboratoryjnej (GLP). SciencePharma dysponuje do\u015bwiadczonym zespo\u0142em audytor\u00f3w posiadaj\u0105cych szerok\u0105 wiedz\u0119 w zakresie prowadzenia nieklinicznych bada\u0144 in vitro i in vivo oraz wykonywania analiz pr\u00f3bek pobranych od uczestnik\u00f3w bada\u0144 klinicznych zar\u00f3wno metodami [&hellip;]<\/p>\n","protected":false},"featured_media":0,"template":"","meta":{"inline_featured_image":false},"taxonomy":[90,100],"class_list":["post-7285","pharmacovigilance","type-pharmacovigilance","status-publish","hentry","taxonomy-audyty-gxp-pl","taxonomy-glp"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.8 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>GLP - SciencePharma<\/title>\n<meta name=\"description\" content=\"W celu zapewnienia jako\u015bci bada\u0144 nieklinicznych oraz oznacze\u0144 bioanalitycznych w badaniach klinicznych wszystkie wymienione badania powinny by\u0107 prowadzone zgodnie z zasadami Dobrej Praktyki Laboratoryjnej (GLP).\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.sciencepharma.com\/pl\/services\/glp\/\" \/>\n<meta property=\"og:locale\" content=\"pl_PL\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"GLP - 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