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Pharmaceutical sciences / European Medicines Agency / EudraVigilance / EudraCT / Clinical trial / Clinical Trials Directive / Good Clinical Practice / Ethics Committee / EudraLex / Clinical research / Research / Health


08 January 2010 EMA[removed]European Medicines Agency response to the European Commission’s “ASSESSMENT OF THE FUNCTIONING OF THE “CLINICAL TRIALS DIRECTIVE” [removed]EC” launched in October 2009.
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Document Date: 2013-10-09 09:33:24

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City

London / /

Company

EudraVigilance Expert Working Group / /

Continent

Europe / /

Country

United Kingdom / /

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Facility

Canary Wharf / /

IndustryTerm

clinical trial protocol / pharmaceutical development / investigational medicinal product / active substances/medicinal products / less well known products / well characterised products / status applications / ad hoc working / insurance/indemnity / medicinal products / /

MedicalCondition

disease / /

Organization

National Institute of Health / World Health Organization / European Union / European Medicines Agency / E-mail info@ema.europa.eu Website www.ema.europa.eu An / European Commission / /

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Technology

clinical trial protocol / /

URL

www.ema.europa.eu / /

SocialTag