Wi\u0119cej<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"PhV Nowe przepisy prawne dotycz\u0105ce nadzoru nad bezpiecze\u0144stwem farmakoterapii z\u00a0lipca 2012 roku wprowadzi\u0142y wymogi prawne dla\u00a0podmiotu odpowiedzialnego dotycz\u0105ce przeprowadzania regularnych audyt\u00f3w ich systemu nadzoru nad bezpiecze\u0144stwem farmakoterapii – Pharmacovigilance, opartych na analizie ryzyka. Wskaz\u00f3wki dotycz\u0105ce planowania i\u00a0przeprowadzania wymaganych prawem audyt\u00f3w zawarte s\u0105\u00a0w\u00a0wytycznych w\u00a0sprawie dobrej praktyki nadzoru nad bezpiecze\u0144stwem farmakoterapii (ang.\u00a0Good Pharmacovigilance Practice,\u00a0GVP Modu\u0142 IV) Europejskiej […]<\/p>\n","protected":false},"featured_media":0,"template":"","meta":{"inline_featured_image":false},"taxonomy":[90,122],"class_list":["post-7445","pharmacovigilance","type-pharmacovigilance","status-publish","hentry","taxonomy-audyty-gxp-pl","taxonomy-phv1"],"acf":[],"yoast_head":"\n
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