B.08 GUIMA Transfer national requirements AT BE CZ DE(BVL, PEI) EE ES FI FR IE IS IT LT LV NL PL RO SE SK SI UKEMA-CMDv

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Date: 2016-02-02 09:57:36 Pharmaceuticals policy Health care Health Pharmaceutical industry Medical research Healthcare quality European Medicines Agency European Union Qualified Person Responsible For Pharmacovigilance Marketing authorization Summary of Product Characteristics Pharmacovigilance		B.08 GUIMA Transfer national requirements AT BE CZ DE(BVL, PEI) EE ES FI FR IE IS IT LT LV NL PL RO SE SK SI UKEMA-CMDv Add to Reading List Source URL: www.hma.eu Download Document from Source Website File Size: 225,29 KB Share Document on Facebook

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