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European Medicines Agency / Good Clinical Practice Directive / EudraLex / Ethics Committee / Good Clinical Practice / Clinical trial / EudraCT / Institutional review board / Good Laboratory Practice / Clinical research / Research / Clinical Trials Directive


Document Date: 2013-10-09 09:00:29

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City

Helsinki / Bruxelles / Brussels / /

Country

Norway / Belgium / Iceland / Liechtenstein / /

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IndustryTerm

pharmaceutical form / civil law / pharmaceuticals / investigational medicinal product / non-modified medicinal product / obligatory insurance coverage stop / manufacturing practices / medicinal product / trial protocol / authorised medicinal product / manufacturing / criminal law / i.e. travel costs / http /

MedicalCondition

bodily injury / /

MusicGroup

Yes / /

Organization

EUROPEAN COMMISSION ENTERPRISE AND INDUSTRY DIRECTORATE / European Medicines Agency / national competent authority / EUROPEAN COMMISSION / European Court of Justice / European Union / European Parliament / Ethics Committee / /

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Position

INVESTIGATOR / principal investigator / The sponsor/investigator / central legal representative / REPRESENTATIVE / legal representative / /

ProgrammingLanguage

EC / /

Technology

trial protocol / /

URL

http /

SocialTag