View source for Document:EU 2011/C 172/01 - CT-3 11-Jun-2011

{{DocumentData
|reference=EU  2011/C 172/01 -
CT-3  11-Jun-2011
|validity_area=EU
|scopes=G
|doc_name=2011/C 172/01 -
CT-3
|version=11-Jun-2011
|status=Current
|doc_type=Regulatory requirement
|language=EN
|description=Communication from the Commission — 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’ )
|official_link=https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=oj:JOC_2011_172_R_0001_01
|restricted=No
|submitted_by=Florian Adragna
|contributors=
}}