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REGULATION on Marketing Authorisations for Proprietary Medicinal Products, their Labelling and Package Leaflets, No[removed], as amended by Regulations No[removed]and No[removed]
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Document Date: 2013-06-12 06:10:44


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File Size: 302,08 KB

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Iceland / /

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Product Issues / Product Recall / /

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pharmaceutical form / Generic medicinal product / reference medicinal product / opened medicinal products / orphan medicinal product / blood products / biological medicinal product / homeopathic medicinal products / machinery / veterinary medicinal products / Physical and chemical data / manufacturing license / pharmaceutical manufacturing facility / chemical products / chemical reaction / manufacturing practice / suitable medicinal product / food-producing animal species / medicinal products / immunological medicinal product / manufacturing process / homeopathic manufacturing procedure / authorised manufacturer / immunological veterinary medicinal product / allergen products / chemical description / pharmaceutical forms / chemical name / medicinal product / immunological veterinary medicinal products / chemical materials / chemical / immunological medicinal products / slaughter products / veterinary medical product / chemical agents / veterinary medicinal product / Ready-to-use medicinal products / homeopathic medicinal product / ready-to-use medicinal product / human blood products / orphan medicinal products / ready-to-use pharmaceutical / /

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smallpox / diphtheria / polio vaccine / illness / serious epidemics / diseases / cholera / /

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European Medical Agency / Icelandic Medicines Agency / European Parliament / World Health Organisation / European Medicines Agency / US Federal Reserve / European Commission / EU Commission / European Pharmacopoeia Commission / EFTA Surveillance Authority / European Union / /

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Dick Tests / /

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veterinarian / physician / General / Any physician / A. General / author / dentist / representative / /

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period / /

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EC / /

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radiation / radiopharmaceuticals / pharmacokinetics / pharmacodynamics / /

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