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London, 20 November 2008 - European Commission
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London, 20 November 2008 - European Commission
Website URL:
http://ec.europa.eu/health/files/eudralex/vol-2/c/smpc_guideline_rev2_en.pdf
Category:
Digital Art
If a diluent is part of the medicinal product, information should be included in the relevant sections (usually sections 3, 6.1, 6.5 and 6.6). Qualitative declaration
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