Generic_exemptions_authorisation_en

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European Union Law Directive 2001/83/EC Health Biocidal Products Directive Directive 93/41/EEC Good Laboratory Practice Pharmaceuticals policy Clinical research European Union directives		Generic_exemptions_authorisation_en Add to Reading List Source URL: echa.europa.eu Download Document from Source Website File Size: 131,39 KB Share Document on Facebook

	Internal Market Information System (IMI) The European Union, in order to facilitate the professional activities of its citizens in other Member States, has enacted two relevant Directives, concerning the recognition of p DocID: 1uU9A - View Document
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