Management of safety information from clinical trials : report of CIOMS Working Group VI.
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TextPublication details: Geneva : CIOMS, 2005. Description: 303 pISBN: 9290360798Other title: [Portion of title]Subject(s): Clinical trials -- ethics -- standards | Adverse drug reaction reporting systems -- standards -- legislation | Product surveillance, Postmarketing -- standards | Data collection -- standards | Safety management -- methods | Risk assessment | Pharmaceuticals and BiologicalsNLM classification: QV 771 2005CI
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