Guideline

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Detailed guidance on the collection, verification and presentation of adverse event/reaction reports arising from clinical trials on medicinal products for human use (‘CT-3’
Short Title:	Detailed guidance on the collection, verification and presentat
Internet:	http://ec.europa.eu/health/files/eudralex/vol-10/2011_c172_01/2011_c172_01_en.pdf
Origin/Publisher:	Official Journal of the European Union
Content:	Detailed guidance on the collection, verification and presentation of adverse event/reaction reports arising from clinical trials on medicinal products for human use (‘CT-3’)
Status:	Revision 2
Document Type:	Guidance