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Pharmacology / Test data exclusivity / Orphan drug / Directive 65/65/EEC / Directive 75/319/EEC / European Medicines Agency / Supplementary protection certificate / Pharmaceuticals policy / Health / Pharmaceutical sciences


BEST PRACTICE GUIDE FOR THE EXCHANGE OF REGULATORY AND ADMINISTRATIVE INFORMATION REGARDING ORPHAN MEDICINAL PRODUCTS BETWEEN THE EMEAEMA AND THE NATIONAL COMPETENT AUTHORITIES October 2003
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Document Date: 2011-11-25 05:34:30


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