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Pharmaceuticals policy / Pharmacy / Health / Pharmacovigilance / Test data exclusivity / Audio power / Pharmaceutical sciences / Pharmacology / Drug safety


Q/A-LIST FOR THE SUBMISSION OF VARIATIONS ACCORDING TO COMMISSION REGULATION (ECDoc. Ref: CMDhRev.33 March.
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Document Date: 2015-04-01 08:54:15

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duplicate applications / medicinal product / topical solutions / valid manufacturing authorisation / manufacturing sites / manufacturing site / informed consent applications / finished product / oral pharmaceutical forms / medicinal products / oral pharmaceutical form / pharmaceutical forms / variation applications / /

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European Directorate for the Quality of Medicines / /

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C / /

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Iowa / Massachusetts / /

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Core / /

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